Canonical Allele Identifier: PA2826006556
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 635731

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159395.1:p.Ser36Phe
CA8519156
NM_001165923.4:c.107C>T