Canonical Allele Identifier: PA2827434785
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335149.1:p.Arg551Trp
CA254160
NM_001348220.1:c.1651C>T