Allele Registry

Canonical Allele Identifier: PA2826006802

Gene: HNF1B HGNC NCBI

ClinVar RCV:

RCV000030535

RCV001852607

ClinVar Variation:

36854

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159395.1:p.Ala291Ser	CA214369 NM_001165923.4:c.871G>T