Canonical Allele Identifier: PA112572
Gene: ALPL HGNC NCBI

Linked Data

ClinVar Variation Id: 13667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000469.3:p.Ala33Val
CA256924
NM_000478.6:c.98C>T