Canonical Allele Identifier: PA2826888796
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 2872756
ClinVar RCV Id: RCV003707038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291215.1:p.Thr64Ser
CA8519134
NM_001304286.2:c.191C>G
CA398753981
NM_001304286.2:c.190A>T