Allele Registry

Canonical Allele Identifier: PA2828455638

Gene: FECH HGNC NCBI

ClinVar RCV:

RCV000000579

RCV001794424

ClinVar Variation:

549

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358024.1:p.Met195Ile	CA251505 NM_001371095.1:c.585G>A CA300835076 NM_001371095.1:c.585G>T CA402535565 NM_001371095.1:c.585G>C