Canonical Allele Identifier: PA203456
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 198451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073991.2:p.Ser117Arg
CA203454
NM_001080522.2:c.351T>G
CA356408266
NM_001080522.2:c.349A>C
CA356408272
NM_001080522.2:c.351T>A