Canonical Allele Identifier: PA2827663797
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 203879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339535.1:p.Val110Leu
CA312817
NM_001352606.2:c.328G>C