Allele Registry

Canonical Allele Identifier: PA263492

Gene: PPT1 HGNC NCBI

ClinVar RCV:

RCV000049598

ClinVar Variation:

56187

HGVS (amino-acid)	Matching Registered Transcripts
NP_000301.1:p.Gln91Pro	CA263490 NM_000310.4:c.272A>C