Canonical Allele Identifier: PA2828455511
Gene: FECH HGNC NCBI

Linked Data

ClinVar Variation Id: 327428
ClinVar RCV Id: RCV000332701

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358023.1:p.Gln252Arg
CA8973074
NM_001371094.1:c.755A>G