Allele Registry

Canonical Allele Identifier: PA112786

Gene: ALPL HGNC NCBI

ClinVar RCV:

RCV000014672

RCV000169778

RCV000710510

RCV001194283

RCV001253058

ClinVar Variation:

13679

HGVS (amino-acid)	Matching Registered Transcripts
NP_000469.3:p.Asn417Ser	CA199266 NM_000478.6:c.1250A>G