Allele Registry

Canonical Allele Identifier: PA2580139551

Gene: FAM229B HGNC NCBI

ClinVar RCV:

RCV004175707

ClinVar Variation:

2335953

HGVS (amino-acid)	Matching Registered Transcripts
NP_001028736.1:p.Ser30Arg	CA365361850 NM_001033564.3:c.88A>C CA365361856 NM_001033564.3:c.90T>A CA365361857 NM_001033564.3:c.90T>G