Canonical Allele Identifier: PA2827663309
Gene: PCCA HGNC NCBI

Linked Data

ClinVar Variation Id: 845962
ClinVar RCV Id: RCV001049142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339534.1:p.Glu302Gln
CA388694636
NM_001352605.2:c.904G>C