Canonical Allele Identifier: PA2825060571
Gene: FECH HGNC NCBI

Linked Data

ClinVar Variation Id: 3094360
ClinVar RCV Id: RCV004391714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000131.2:p.Pro67Leu
CA8973277
NM_000140.5:c.200C>T