Canonical Allele Identifier: PA214366
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 36852

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000449.1:p.Val25Leu
CA214365
NM_000458.4:c.73G>T
CA398754761
NM_000458.4:c.73G>C