Allele Registry

Canonical Allele Identifier: PA2826888834

Gene: HNF1B HGNC NCBI

ClinVar RCV:

RCV002880952

ClinVar Variation:

2029702

HGVS (amino-acid)	Matching Registered Transcripts
NP_001291215.1:p.Asn146Lys	CA398751451 NM_001304286.2:c.438C>G CA398751453 NM_001304286.2:c.438C>A