Allele Registry

Canonical Allele Identifier: PA2828455409

Gene: FECH HGNC NCBI

ClinVar RCV:

RCV002115711

RCV003923632

ClinVar Variation:

1599190

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358023.1:p.Gly55Ser	CA8973304 NM_001371094.1:c.163G>A