Canonical Allele Identifier: PA111325
Gene: FECH HGNC NCBI
ClinVar RCV:
RCV000000584
ClinVar Variation:
554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000131.2:p.Val362Gly
CA251512
NM_000140.5:c.1085T>G