Canonical Allele Identifier: PA2573075606
Gene: CC2D2A HGNC NCBI

Linked Data

ClinVar Variation Id: 743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365544.1:p.Pro1122Ser
CA114469
NM_001378615.1:c.3364C>T