Canonical Allele Identifier: PA2826006585
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 635723
ClinVar RCV Id: RCV000787242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159395.1:p.Glu78Asp
CA398753631
NM_001165923.4:c.234G>T
CA398753634
NM_001165923.4:c.234G>C