Allele Registry

Canonical Allele Identifier: PA645375570

Gene: FA2H HGNC NCBI

ClinVar Allele:

360397

ClinVar RCV:

RCV000413571

RCV001336096

RCV001337611

ClinVar Variation:

372860

HGVS (amino-acid)	Matching Registered Transcripts
NP_077282.3:p.Glu47Lys	CA16043088 NM_024306.5:c.139G>A