Allele Registry

Canonical Allele Identifier: PA2573073294

Gene: FECH HGNC NCBI

ClinVar Allele:

331897

ClinVar RCV:

RCV000285620

RCV001521397

ClinVar Variation:

327434

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361707.1:p.Arg96Gln	CA8973261 NM_001374778.1:c.287G>A