Allele Registry

Canonical Allele Identifier: PA2828455465

Gene: FECH HGNC NCBI

ClinVar RCV:

RCV000023941

ClinVar Variation:

30951

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358023.1:p.Ala185Thr	CA259953 NM_001371094.1:c.553G>A