Canonical Allele Identifier: PA2827665032
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 203880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339537.1:p.Gly116Asp
CA312819
NM_001352608.2:c.347G>A