Allele Registry

Canonical Allele Identifier: PA2573075620

Gene: CC2D2A HGNC NCBI

ClinVar Allele:

489382

ClinVar RCV:

RCV000594861

RCV000694442

RCV000765756

RCV001148070

RCV001148071

ClinVar Variation:

497958

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365544.1:p.Thr649Met	CA2863798 NM_001378615.1:c.1946C>T