Allele Registry

Canonical Allele Identifier: PA111265

Gene: FECH HGNC NCBI

ClinVar RCV:

RCV000416464

RCV001861467

ClinVar Variation:

375409

HGVS (amino-acid)	Matching Registered Transcripts
NP_000131.2:p.Pro334Leu	CA8973020 NM_000140.5:c.1001C>T