Allele Registry

Canonical Allele Identifier: PA645468081

Gene: FECH HGNC NCBI

ClinVar RCV:

RCV000332701

ClinVar Variation:

327428

HGVS (amino-acid)	Matching Registered Transcripts
NP_001012533.1:p.Gln291Arg	CA8973074 NM_001012515.4:c.872A>G