Canonical Allele Identifier: PA916035559
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 498769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339538.1:p.Met316Arg
CA388694737
NM_001352609.2:c.947T>G