Canonical Allele Identifier: PA112659
Gene: ALPL HGNC NCBI

Linked Data

ClinVar Variation Id: 381586

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000469.3:p.Arg223Gln
CA666577
NM_000478.6:c.668G>A