Canonical Allele Identifier: PA2827432098
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335143.1:p.Arg415Trp
CA254160
NM_001348214.2:c.1243C>T