Canonical Allele Identifier: PA2826320273
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230157.1:p.Arg586Trp
CA254160
NM_001243228.2:c.1756C>T