Canonical Allele Identifier: PA2828455713
Gene: FECH HGNC NCBI
ClinVar RCV:
RCV000000581
ClinVar Variation:
551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358024.1:p.Phe345Ser
CA251508
NM_001371095.1:c.1034T>C