Allele Registry

Canonical Allele Identifier: PA259955

Gene: FECH HGNC NCBI

ClinVar RCV:

RCV000023941

ClinVar Variation:

30951

HGVS (amino-acid)	Matching Registered Transcripts
NP_001012533.1:p.Ala191Thr	CA259953 NM_001012515.4:c.571G>A