Canonical Allele Identifier: PA210255
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 217610

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073991.2:p.Leu559Pro
CA210253
NM_001080522.2:c.1676T>C