Allele Registry

Canonical Allele Identifier: PA112842

Gene: ALPL HGNC NCBI

ClinVar RCV:

RCV000014661

RCV000014662

RCV000207084

RCV000224520

RCV000763302

RCV001847606

RCV004549364

ClinVar Variation:

13671

HGVS (amino-acid)	Matching Registered Transcripts
NP_000469.3:p.Asp378Val	CA256928 NM_000478.6:c.1133A>T