Canonical Allele Identifier: PA2741888600
Gene: FTH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2833850
ClinVar RCV Id: RCV003692207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002023.2:p.Leu149Val
CA380854033
NM_002032.3:c.445T>G