Allele Registry

Canonical Allele Identifier: PA105019

Gene: HFE HGNC NCBI

ClinVar RCV:

RCV001757420

RCV002300585

RCV003125900

ClinVar Variation:

1315973

HGVS (amino-acid)	Matching Registered Transcripts
NP_000401.1:p.Arg66Cys	CA3666607 NM_000410.4:c.196C>T