Canonical Allele Identifier: PA2825060577
Gene: FECH HGNC NCBI

Linked Data

ClinVar Variation Id: 992439
ClinVar RCV Id: RCV001280888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000131.2:p.Gly77Arg
CA402537043
NM_000140.5:c.229G>A
CA402537045
NM_000140.5:c.229G>C