ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826006748
Gene: HNF1B
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV002464053
RCV003103168
ClinVar Variation:
1801843
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001159395.1:p.Arg226Gln
CA8519014
NM_001165923.4:c.677G>A