Allele Registry

Canonical Allele Identifier: PA112887

Gene: ALPL HGNC NCBI

ClinVar RCV:

RCV000418683

RCV002278676

ClinVar Variation:

381585

HGVS (amino-acid)	Matching Registered Transcripts
NP_000469.3:p.Gln76Arg	CA16603529 NM_000478.6:c.227A>G