Canonical Allele Identifier: PA2573075652
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 217601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Val996Ala
CA279522
NM_001378617.1:c.2987T>C