Canonical Allele Identifier: PA2826131620
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 498769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171475.1:p.Met316Arg
CA388694737
NM_001178004.2:c.947T>G