Canonical Allele Identifier: PA916006351
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230155.2:p.Ala716Val
CA402528341
NM_001243226.3:c.2147C>T