Canonical Allele Identifier: PA2826006636
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 635704
ClinVar RCV Id: RCV000787218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159395.1:p.His132Pro
CA398751611
NM_001165923.4:c.395A>C