Allele Registry

Canonical Allele Identifier: PA214374

Gene: HNF1B HGNC NCBI

ClinVar RCV:

RCV000030537

RCV001844804

ClinVar Variation:

36856

HGVS (amino-acid)	Matching Registered Transcripts
NP_000449.1:p.Asn321Ser	CA214373 NM_000458.4:c.962A>G