Canonical Allele Identifier: PA2826006628
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 595969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159395.1:p.Ala122Thr
CA398751718
NM_001165923.4:c.364G>A