Allele Registry

Canonical Allele Identifier: PA2573075590

Gene: CC2D2A HGNC NCBI

ClinVar Variation Id: 347842

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365544.1:p.Phe911Leu	CA2863998 NM_001378615.1:c.2731T>C CA356412335 NM_001378615.1:c.2733T>A CA356412336 NM_001378615.1:c.2733T>G