Canonical Allele Identifier: PA2826006780
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 288154
ClinVar RCV Id: RCV000787122 RCV000713806 RCV001535983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159395.1:p.Arg269His
CA10605981
NM_001165923.4:c.806G>A