Canonical Allele Identifier: PA2827663161
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 203880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339534.1:p.Gly142Asp
CA312819
NM_001352605.2:c.425G>A