Canonical Allele Identifier: PA2827663341
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 3023607
ClinVar RCV Id: RCV003880702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339534.1:p.Val321Ala
CA388694769
NM_001352605.2:c.962T>C