Canonical Allele Identifier: PA645509549
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 438661
ClinVar RCV Id: RCV000505626 RCV002464229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291215.1:p.Gly440Glu
CA398750158
NM_001304286.2:c.1319G>A