Allele Registry

Canonical Allele Identifier: PA645468096

Gene: FECH HGNC NCBI

ClinVar RCV:

RCV000285620

RCV001521397

ClinVar Variation:

327434

HGVS (amino-acid)	Matching Registered Transcripts
NP_000131.2:p.Arg96Gln	CA8973261 NM_000140.5:c.287G>A