Canonical Allele Identifier: PA2827432127
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1706281
ClinVar RCV Id: RCV002284811
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335143.1:p.Leu446Pro
CA402528415
NM_001348214.2:c.1337T>C