Canonical Allele Identifier: PA2825145507
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 2502223
ClinVar RCV Id: RCV003228641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000449.1:p.Lys4Arg
CA398755386
NM_000458.4:c.11A>G