Canonical Allele Identifier: PA2825185049
Gene: ALPL HGNC NCBI

Linked Data

ClinVar Variation Id: 1496773
ClinVar RCV Id: RCV001992047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000469.3:p.Met89Ile
CA666439
NM_000478.6:c.267G>A
CA338878155
NM_000478.6:c.267G>C
CA338878157
NM_000478.6:c.267G>T