Allele Registry

Canonical Allele Identifier: PA259954

Gene: FECH HGNC NCBI

ClinVar RCV:

RCV000023941

ClinVar Variation:

30951

HGVS (amino-acid)	Matching Registered Transcripts
NP_000131.2:p.Ala185Thr	CA259953 NM_000140.5:c.553G>A