Canonical Allele Identifier: PA2827431089
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 432062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335141.1:p.Ser123Arg
CA402701458
NM_001348212.2:c.369C>G
CA402701459
NM_001348212.2:c.369C>A
CA402701465
NM_001348212.2:c.367A>C