Allele Registry

Canonical Allele Identifier: PA214347

Gene: HNF1B HGNC NCBI

ClinVar RCV:

RCV000030520

RCV002464083

ClinVar Variation:

36839

HGVS (amino-acid)	Matching Registered Transcripts
NP_000449.1:p.Met442Thr	CA214346 NM_000458.4:c.1325T>C