Canonical Allele Identifier: PA2826321462
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 432062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230161.1:p.Ser182Arg
CA402701458
NM_001243232.1:c.546C>G
CA402701459
NM_001243232.1:c.546C>A
CA402701465
NM_001243232.1:c.544A>C