Canonical Allele Identifier: PA645445472
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 322943
ClinVar RCV Id: RCV000343034 RCV000445437 RCV001613036
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291215.1:p.Phe443Leu
CA8518750
NM_001304286.2:c.1329T>G
CA398750135
NM_001304286.2:c.1329T>A
CA398750140
NM_001304286.2:c.1327T>C