Canonical Allele Identifier: PA913193060
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 635723
ClinVar RCV Id: RCV000787242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000449.1:p.Glu78Asp
CA398753631
NM_000458.4:c.234G>T
CA398753634
NM_000458.4:c.234G>C