Allele Registry

Canonical Allele Identifier: PA105062

Gene: HFE HGNC NCBI

ClinVar Allele:

15058

ClinVar RCV:

RCV000000036

RCV001050090

RCV003884332

ClinVar Variation:

HGVS (amino-acid)	Matching Registered Transcripts
NP_000401.1:p.Gln283Pro	CA280949 NM_000410.4:c.848A>C