Canonical Allele Identifier: PA2827664095
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 92761

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339535.1:p.Ile427Val
CA145988
NM_001352606.2:c.1279A>G