Canonical Allele Identifier: PA2827432205
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 432062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335144.1:p.Ser37Arg
CA402701458
NM_001348215.2:c.111C>G
CA402701459
NM_001348215.2:c.111C>A
CA402701465
NM_001348215.2:c.109A>C