Allele Registry

Canonical Allele Identifier: PA2825811683

Gene: FAM111B HGNC NCBI

ClinVar RCV:

RCV000106319

ClinVar Variation:

120219

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136176.1:p.Ser598Asn	CA150787 NM_001142704.1:c.1793G>A