Canonical Allele Identifier: PA2573075576
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 194821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365544.1:p.Pro721Ser
CA201373
NM_001378615.1:c.2161C>T