Allele Registry

Canonical Allele Identifier: PA645375623

Gene: FA2H HGNC NCBI

ClinVar Allele:

242500

ClinVar RCV:

RCV000419332

RCV000514460

RCV001084384

RCV001115913

RCV001848010

ClinVar Variation:

241461

HGVS (amino-acid)	Matching Registered Transcripts
NP_077282.3:p.Arg113Gln	CA8170581 NM_024306.5:c.338G>A