Canonical Allele Identifier: PA1139684783
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_001012533.1:p.Gly83Arg
CA402537043
NM_001012515.4:c.247G>A
CA402537045
NM_001012515.4:c.247G>C