Allele Registry

Canonical Allele Identifier: PA113799

Gene: HFE HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000000026

RCV000175607

RCV000394716

RCV000763144

RCV000844708

RCV000991133

RCV001248831

RCV001731265

RCV002227011

RCV002272003

ClinVar Variation:

10

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000401.1:p.His63Asp	CA113797 NM_000410.4:c.187C>G