Allele Registry

Canonical Allele Identifier: PA2826006629

Gene: HNF1B HGNC NCBI

ClinVar Variation Id: 635708

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159395.1:p.Met124Ile	CA398751696 NM_001165923.4:c.372G>A CA398751697 NM_001165923.4:c.372G>C CA398751698 NM_001165923.4:c.372G>T