Canonical Allele Identifier: PA915956378
Gene: FECH HGNC NCBI
ClinVar RCV:
RCV000000589
ClinVar Variation:
559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001012533.1:p.Asn69Asp
CA251520
NM_001012515.4:c.205A>G