Allele Registry

Canonical Allele Identifier: PA2826006608

Gene: HNF1B HGNC NCBI

ClinVar RCV:

RCV002895553

ClinVar Variation:

2042436

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159395.1:p.Glu101Gln	CA8519119 NM_001165923.4:c.301G>C