Allele Registry

SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-09-25T08:00:00-0500
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Canonical Allele Identifier: PA2580260971

Gene: CTSD HGNC NCBI

Linked Data

ClinVar Variation Id: 2110822

ClinVar RCV Id: RCV003020340

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001900.1:p.Asp306Glu	CA379093803 NM_001909.5:c.918T>G CA379093805 NM_001909.5:c.918T>A