Allele Registry

Canonical Allele Identifier: PA210289

Gene: CC2D2A HGNC NCBI

ClinVar Allele:

214193

ClinVar RCV:

RCV000201634

RCV000541700

ClinVar Variation:

217614

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073991.2:p.Leu1534Val	CA210287 NM_001080522.2:c.4600T>G