Allele Registry

Canonical Allele Identifier: PA012203

Gene: FECH HGNC NCBI

ClinVar RCV:

RCV001857788

ClinVar Variation:

242756

HGVS (amino-acid)	Matching Registered Transcripts
NP_001012533.1:p.Cys417Gly	CA006500 NM_001012515.4:c.1249T>G