Canonical Allele Identifier: PA2573075645
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 217604
ClinVar Variation Id: 1453471
ClinVar RCV Id: RCV002037916

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Glu951Val
CA210338
NM_001378617.1:c.2852A>T
CA2573137613
NM_001378617.1:c.2852_2853delinsTT