Allele Registry

Canonical Allele Identifier: PA916071729

Gene: HFE HGNC NCBI

ClinVar RCV:

RCV000000029

RCV001322296

ClinVar Variation:

HGVS (amino-acid)	Matching Registered Transcripts
NP_620578.1:p.Ile82Thr	CA280941 NM_139009.3:c.245T>C