Allele Registry

Canonical Allele Identifier: PA2825312571

Gene: FECH HGNC NCBI

ClinVar Allele:

331897

ClinVar RCV:

RCV000285620

RCV001521397

ClinVar Variation:

327434

HGVS (amino-acid)	Matching Registered Transcripts
NP_001012533.1:p.Arg102Gln	CA8973261 NM_001012515.4:c.305G>A