Canonical Allele Identifier: PA2828787727
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 56307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Trp1133Arg
CA144229
NM_001378617.1:c.3397T>C
CA356421950
NM_001378617.1:c.3397T>A