Canonical Allele Identifier: PA2828348489
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 432062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356505.1:p.Ser228Arg
CA402701458
NM_001369576.1:c.684C>G
CA402701459
NM_001369576.1:c.684C>A
CA402701465
NM_001369576.1:c.682A>C