Allele Registry

Canonical Allele Identifier: PA251506

Gene: FECH HGNC NCBI

ClinVar RCV:

RCV000000579

RCV001794424

ClinVar Variation:

549

HGVS (amino-acid)	Matching Registered Transcripts
NP_001012533.1:p.Met273Ile	CA251505 NM_001012515.4:c.819G>A CA300835076 NM_001012515.4:c.819G>T CA402535565 NM_001012515.4:c.819G>C