Canonical Allele Identifier: PA916035553
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218252

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339538.1:p.Gln293Arg
CA10575828
NM_001352609.2:c.878A>G