Canonical Allele Identifier: PA891863512
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 591835
ClinVar RCV Id: RCV000723017 RCV003235374
ClinVar Variation Id: 1802529
ClinVar RCV Id: RCV002465370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000449.1:p.Gly20Arg
CA290293293
NM_000458.4:c.58G>C
CA398754853
NM_000458.4:c.58G>A