Canonical Allele Identifier: PA2828455424
Gene: FECH HGNC NCBI

Linked Data

ClinVar Variation Id: 327435
ClinVar RCV Id: RCV000342940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358023.1:p.Lys68Glu
CA8973274
NM_001371094.1:c.202A>G