Allele Registry

Canonical Allele Identifier: PA2828548480

Gene: FECH HGNC NCBI

ClinVar RCV:

RCV001857788

ClinVar Variation:

242756

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361707.1:p.Cys391Gly	CA006500 NM_001374778.1:c.1171T>G