Canonical Allele Identifier: PA2826319051
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1791142
ClinVar RCV Id: RCV002450449 RCV003098870
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230155.2:p.Thr183Ser
CA8970612
NM_001243226.3:c.548C>G
CA402703575
NM_001243226.3:c.547A>T