Canonical Allele Identifier: PA2827430913
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335140.1:p.Arg538Trp
CA254160
NM_001348211.2:c.1612C>T