Allele Registry

Canonical Allele Identifier: PA2826006747

Gene: HNF1B HGNC NCBI

ClinVar RCV:

RCV000479017

RCV000787150

ClinVar Variation:

418253

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159395.1:p.Arg226Pro	CA16620399 NM_001165923.4:c.677G>C