Allele Registry

Canonical Allele Identifier: PA111156

Gene: FECH HGNC NCBI

ClinVar RCV:

RCV000000578

RCV000455178

RCV001517622

ClinVar Variation:

548

HGVS (amino-acid)	Matching Registered Transcripts
NP_000131.2:p.Gly55Cys	CA251503 NM_000140.5:c.163G>T