Allele Registry

Canonical Allele Identifier: PA645375752

Gene: FA2H HGNC NCBI

ClinVar RCV:

RCV000414400

RCV001861420

ClinVar Variation:

372861

HGVS (amino-acid)	Matching Registered Transcripts
NP_077282.3:p.His261Arg	CA8170413 NM_024306.5:c.782A>G