Canonical Allele Identifier: PA2830270043
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 959749
ClinVar RCV Id: RCV001233153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620573.1:p.Asp150Asn
CA136292908
NM_139004.3:c.448G>A