Canonical Allele Identifier: PA113799
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 10
ClinVar RCV Id: RCV000000026 RCV000175607 RCV000394716 RCV000763144 RCV000991133 RCV000844708 RCV001248831 RCV001731265 RCV002227011 RCV002272003
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Amino-acid Alleles

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