Allele Registry

Canonical Allele Identifier: PA2828455712

Gene: FECH HGNC NCBI

ClinVar RCV:

RCV001857788

ClinVar Variation:

242756

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358024.1:p.Cys339Gly	CA006500 NM_001371095.1:c.1015T>G