Allele Registry

Canonical Allele Identifier: PA2828548456

Gene: FECH HGNC NCBI

ClinVar RCV:

RCV000332701

ClinVar Variation:

327428

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361707.1:p.Gln285Arg	CA8973074 NM_001374778.1:c.854A>G