Canonical Allele Identifier: PA2827666619
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 92761

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339541.1:p.Ile112Val
CA145988
NM_001352612.2:c.334A>G