Canonical Allele Identifier: PA2826002428
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1039410
ClinVar RCV Id: RCV001342873

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158192.1:p.His56Tyr
CA2863296
NM_001164720.1:c.166C>T