Canonical Allele Identifier: PA214349
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 36840
ClinVar RCV Id: RCV000030521 RCV000787252 RCV000730643 RCV002490424
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000449.1:p.Pro47Leu
CA214348
NM_000458.4:c.140C>T