Canonical Allele Identifier: PA658804896
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 498769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000273.2:p.Met316Arg
CA388694737
NM_000282.4:c.947T>G