Canonical Allele Identifier: PA2827433892
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1791142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335148.1:p.Thr57Ser
CA8970612
NM_001348219.2:c.170C>G
CA402703575
NM_001348219.2:c.169A>T