Canonical Allele Identifier: PA658733692
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 495792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000273.2:p.Met316Lys
CA388694736
NM_000282.4:c.947T>A