Allele Registry

Canonical Allele Identifier: PA2828455556

Gene: FECH HGNC NCBI

ClinVar Allele:

38381

ClinVar RCV:

RCV001857788

ClinVar Variation:

242756

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358023.1:p.Cys378Gly	CA006500 NM_001371094.1:c.1132T>G