Canonical Allele Identifier: PA2825653762
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 203880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121164.1:p.Gly116Asp
CA312819
NM_001127692.3:c.347G>A