Canonical Allele Identifier: PA2827433783
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335147.1:p.Arg556Trp
CA254160
NM_001348218.2:c.1666C>T