Canonical Allele Identifier: PA645468069
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_001012533.1:p.Lys74Glu
CA8973274
NM_001012515.4:c.220A>G