Canonical Allele Identifier: PA916019652
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 635703
ClinVar RCV Id: RCV000787217

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291215.1:p.Asn133Ser
CA398751597
NM_001304286.2:c.398A>G