Allele Registry

Canonical Allele Identifier: PA2828455681

Gene: FECH HGNC NCBI

ClinVar RCV:

RCV000416464

RCV001861467

ClinVar Variation:

375409

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358024.1:p.Pro262Leu	CA8973020 NM_001371095.1:c.785C>T