Canonical Allele Identifier: PA2828352272
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_001356512.1:p.Leu583Pro
CA402528415
NM_001369583.1:c.1748T>C