Allele Registry

Canonical Allele Identifier: PA112652

Gene: ALPL HGNC NCBI

ClinVar RCV:

RCV000623730

RCV000674297

RCV001046115

RCV001730702

RCV002279446

RCV003465357

ClinVar Variation:

521379

HGVS (amino-acid)	Matching Registered Transcripts
NP_000469.3:p.Arg184Trp	CA666527 NM_000478.6:c.550C>T