Canonical Allele Identifier: PA105031
Gene: HFE HGNC NCBI

Linked Data

ClinVar Variation Id: 216425
ClinVar RCV Id: RCV000199898 RCV000329080 RCV000684802 RCV002485319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000401.1:p.Arg6Ser
CA338954
NM_000410.4:c.18G>C
CA363202632
NM_000410.4:c.18G>T