Allele Registry

Canonical Allele Identifier: PA112553

Gene: ALPL HGNC NCBI

ClinVar RCV:

RCV000673035

RCV000778223

RCV000806323

RCV001252803

RCV002249400

RCV002271560

RCV002531329

ClinVar Variation:

556961

HGVS (amino-acid)	Matching Registered Transcripts
NP_000469.3:p.Ala177Thr	CA666521 NM_000478.6:c.529G>A