Allele Registry

Canonical Allele Identifier: PA2828455511

Gene: FECH HGNC NCBI

ClinVar RCV:

RCV000332701

ClinVar Variation:

327428

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