Canonical Allele Identifier: PA2827432450
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335144.1:p.Ala398Val
CA402528341
NM_001348215.2:c.1193C>T