Allele Registry

Canonical Allele Identifier: PA645390610

Gene: H3C11 HGNC NCBI

ClinVar RCV:

RCV000420515

RCV000441693

ClinVar Variation:

376437

HGVS (amino-acid)	Matching Registered Transcripts
NP_003524.1:p.Lys28Glu	CA16602872 NM_003533.3:c.82A>G