Canonical Allele Identifier: PA2828786605
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 217610

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Leu510Pro
CA210253
NM_001378617.1:c.1529T>C