Allele Registry

Canonical Allele Identifier: PA006558

Gene: FECH HGNC NCBI

ClinVar RCV:

RCV001857788

ClinVar Variation:

242756

HGVS (amino-acid)	Matching Registered Transcripts
NP_000131.2:p.Cys411Gly	CA006500 NM_000140.5:c.1231T>G