Canonical Allele Identifier: PA2827663300
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218252

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339534.1:p.Gln293Arg
CA10575828
NM_001352605.2:c.878A>G