Canonical Allele Identifier: PA2826006670
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 635691
ClinVar RCV Id: RCV000787202
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159395.1:p.Pro159Leu
CA398751311
NM_001165923.4:c.476C>T