Canonical Allele Identifier: PA2826006668
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 586800
ClinVar RCV Id: RCV000713801 RCV003313973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159395.1:p.Thr158Asn
CA398751323
NM_001165923.4:c.473C>A