Canonical Allele Identifier: PA105093
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 12
ClinVar RCV Id: RCV000000029 RCV001322296
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Amino-acid Alleles

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