Canonical Allele Identifier: PA2826888800
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 2663552
ClinVar RCV Id: RCV003442740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291215.1:p.Glu78Ala
CA398753644
NM_001304286.2:c.233A>C