Allele Registry

Canonical Allele Identifier: PA2826006651

Gene: HNF1B HGNC NCBI

ClinVar RCV:

RCV002880952

ClinVar Variation:

2029702

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159395.1:p.Asn146Lys	CA398751451 NM_001165923.4:c.438C>G CA398751453 NM_001165923.4:c.438C>A