Canonical Allele Identifier: PA2828548456
Gene: FECH HGNC NCBI

Linked Data

ClinVar Variation Id: 327428
ClinVar RCV Id: RCV000332701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361707.1:p.Gln285Arg
CA8973074
NM_001374778.1:c.854A>G