Allele Registry

SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-09-25T08:00:00-0500
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.

Canonical Allele Identifier: PA2828960792

Gene: APP HGNC NCBI

Linked Data

ClinVar Variation Id: 1315088

ClinVar RCV Id: RCV001773282

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372182.1:p.Met615Leu	CA319103456 NM_001385253.1:c.1843A>T CA409806447 NM_001385253.1:c.1843A>C