Canonical Allele Identifier: PA2826006648
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 635700
ClinVar RCV Id: RCV000787213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159395.1:p.Leu145Gln
CA398751468
NM_001165923.4:c.434T>A