Allele Registry

Canonical Allele Identifier: PA2825300742

Gene: FAM209B HGNC NCBI

ClinVar RCV:

RCV004152526

ClinVar Variation:

2302932

HGVS (amino-acid)	Matching Registered Transcripts
NP_001013668.2:p.Ser30Ile	CA409403380 NM_001013646.3:c.89G>T