Allele Registry

Canonical Allele Identifier: PA214358

Gene: HNF1B HGNC NCBI

ClinVar RCV:

RCV000030527

RCV002464085

ClinVar Variation:

36846

HGVS (amino-acid)	Matching Registered Transcripts
NP_000449.1:p.Ser115Asn	CA214357 NM_000458.4:c.344G>A