Canonical Allele Identifier: PA2825060586
Gene: FECH HGNC NCBI

Linked Data

ClinVar Variation Id: 1360747
ClinVar RCV Id: RCV001907162
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000131.2:p.Ile103Leu
CA402536813
NM_000140.5:c.307A>C