Allele Registry

Canonical Allele Identifier: PA645468083

Gene: FECH HGNC NCBI

ClinVar RCV:

RCV000416464

RCV001861467

ClinVar Variation:

375409

HGVS (amino-acid)	Matching Registered Transcripts
NP_001012533.1:p.Pro340Leu	CA8973020 NM_001012515.4:c.1019C>T