Canonical Allele Identifier: PA210260
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 217597

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073991.2:p.Arg1284Cys
CA210258
NM_001080522.2:c.3850C>T