Allele Registry

Canonical Allele Identifier: PA658662838

Gene: FA2H HGNC NCBI

ClinVar Allele:

441927

ClinVar RCV:

RCV000518709

RCV000633034

RCV001310336

RCV001848887

ClinVar Variation:

447318

HGVS (amino-acid)	Matching Registered Transcripts
NP_077282.3:p.Val309Ile	CA8170349 NM_024306.5:c.925G>A