Canonical Allele Identifier: PA2826006574
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 2872756
ClinVar RCV Id: RCV003707038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159395.1:p.Thr64Ser
CA8519134
NM_001165923.4:c.191C>G
CA398753981
NM_001165923.4:c.190A>T