Canonical Allele Identifier: PA2828786821
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 210608

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Val611Ile
CA208880
NM_001378617.1:c.1831G>A