Canonical Allele Identifier: PA2828344939
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 432062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356498.1:p.Ser252Arg
CA402701458
NM_001369569.1:c.756C>G
CA402701459
NM_001369569.1:c.756C>A
CA402701465
NM_001369569.1:c.754A>C