Canonical Allele Identifier: PA916035549
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 218262
ClinVar RCV Id: RCV000236908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339538.1:p.Arg288Lys
CA10575827
NM_001352609.2:c.863G>A