Canonical Allele Identifier: PA916019617
Gene: HNF1B HGNC NCBI

Linked Data

ClinVar Variation Id: 635735
ClinVar RCV Id: RCV000787261
ClinVar Variation Id: 635736
ClinVar RCV Id: RCV000787262
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291215.1:p.Met1Ile
CA398755454
NM_001304286.2:c.3G>T
CA398755455
NM_001304286.2:c.3G>C
CA398755458
NM_001304286.2:c.3G>A