Canonical Allele Identifier: PA645449784
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 432062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077431.1:p.Ser253Arg
CA402701458
NM_001083962.2:c.759C>G
CA402701459
NM_001083962.2:c.759C>A
CA402701465
NM_001083962.2:c.757A>C