Canonical Allele Identifier: PA2580166713
Gene: TCF7L2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2277423
ClinVar RCV Id: RCV002844117
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139755.1:p.Ser180Leu
CA214116535
NM_001146283.2:c.539C>T