Canonical Allele Identifier: PA112546
Gene: ALPL HGNC NCBI

Linked Data

ClinVar Variation Id: 13683

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000469.3:p.Ala176Thr
CA256935
NM_000478.6:c.526G>A