Allele Registry

Canonical Allele Identifier: PA109378

Gene: FAM111B HGNC NCBI

ClinVar RCV:

RCV000106319

ClinVar Variation:

120219

HGVS (amino-acid)	Matching Registered Transcripts
NP_945185.1:p.Ser628Asn	CA150787 NM_198947.4:c.1883G>A