Canonical Allele Identifier: PA312820
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 203880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000273.2:p.Gly142Asp
CA312819
NM_000282.4:c.425G>A