Allele Registry

Canonical Allele Identifier: PA111216

Gene: FECH HGNC NCBI

ClinVar RCV:

RCV000000579

RCV001794424

ClinVar Variation:

549

HGVS (amino-acid)	Matching Registered Transcripts
NP_000131.2:p.Met267Ile	CA251505 NM_000140.5:c.801G>A CA300835076 NM_000140.5:c.801G>T CA402535565 NM_000140.5:c.801G>C