Canonical Allele Identifier: PA916035562
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 92761

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339538.1:p.Ile475Val
CA145988
NM_001352609.2:c.1423A>G