Canonical Allele Identifier: PA2573075608
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 217598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365544.1:p.Val1151Ala
CA279438
NM_001378615.1:c.3452T>C