Canonical Allele Identifier: PA312818
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 203879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000273.2:p.Val110Leu
CA312817
NM_000282.4:c.328G>C