Canonical Allele Identifier: PA2828352002
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 432062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356512.1:p.Ser229Arg
CA402701458
NM_001369583.1:c.687C>G
CA402701459
NM_001369583.1:c.687C>A
CA402701465
NM_001369583.1:c.685A>C