Canonical Allele Identifier: PA2828347758
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_001356503.1:p.Leu606Pro
CA402528415
NM_001369574.1:c.1817T>C