Canonical Allele Identifier: PA2826131446
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 38867
ClinVar RCV Id: RCV000032110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171475.1:p.Ala138Thr
CA343123
NM_001178004.2:c.412G>A