Canonical Allele Identifier: PA645434960
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218252

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000273.2:p.Gln293Arg
CA10575828
NM_000282.4:c.878A>G