Canonical Allele Identifier: PA2828344706
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356497.1:p.Ala614Val
CA402528341
NM_001369568.1:c.1841C>T