Canonical Allele Identifier: PA112879
Gene: ALPL HGNC NCBI

Linked Data

ClinVar Variation Id: 13666

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000469.3:p.Gln207Pro
CA256923
NM_000478.6:c.620A>C