Canonical Allele Identifier: PA2826323023
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 432062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230165.1:p.Ser93Arg
CA402701458
NM_001243236.2:c.279C>G
CA402701459
NM_001243236.2:c.279C>A
CA402701465
NM_001243236.2:c.277A>C