Canonical Allele Identifier: PA2828788355
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 217603
ClinVar RCV Id: RCV000201684

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365546.1:p.Thr1532Ala
CA279482
NM_001378617.1:c.4594A>G