Canonical Allele Identifier: PA2825145521
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 3236187
ClinVar RCV Id: RCV004555443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000449.1:p.Leu30Ser
CA398754638
NM_000458.4:c.89T>C