Canonical Allele Identifier: PA645434956
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218262
ClinVar RCV Id: RCV000236908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000273.2:p.Arg288Lys
CA10575827
NM_000282.4:c.863G>A