Allele Registry

Canonical Allele Identifier: PA105093

Gene: HFE HGNC NCBI

ClinVar RCV:

RCV000000029

RCV001322296

ClinVar Variation:

HGVS (amino-acid)	Matching Registered Transcripts
NP_000401.1:p.Ile105Thr	CA280941 NM_000410.4:c.314T>C