Allele Registry

Canonical Allele Identifier: PA2826006652

Gene: HNF1B HGNC NCBI

ClinVar RCV:

RCV002470589

ClinVar Variation:

1806305

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159395.1:p.Asn146Thr	CA398751457 NM_001165923.4:c.437A>C