Canonical Allele Identifier: PA2827433036
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 432062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335146.1:p.Ser229Arg
CA402701458
NM_001348217.1:c.687C>G
CA402701459
NM_001348217.1:c.687C>A
CA402701465
NM_001348217.1:c.685A>C