Canonical Allele Identifier: PA913193056
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 635729
ClinVar RCV Id: RCV000787253
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000449.1:p.Glu44Lys
CA398754352
NM_000458.4:c.130G>A