Canonical Allele Identifier: PA913193079
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 635703
ClinVar RCV Id: RCV000787217

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000449.1:p.Asn133Ser
CA398751597
NM_000458.4:c.398A>G