Allele Registry

Canonical Allele Identifier: PA2826888970

Gene: HNF1B HGNC NCBI

ClinVar RCV:

RCV000421527

ClinVar Variation:

377055

HGVS (amino-acid)	Matching Registered Transcripts
NP_001291215.1:p.His310Asn	CA8518951 NM_001304286.2:c.928C>A