Allele Registry

Canonical Allele Identifier: PA2580146542

Gene: FAM124B HGNC NCBI

ClinVar RCV:

RCV004166990

ClinVar Variation:

2323812

HGVS (amino-acid)	Matching Registered Transcripts
NP_001116251.1:p.Cys435Arg	CA351129057 NM_001122779.2:c.1303T>C