Canonical Allele Identifier: PA2827430938
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 393171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335140.1:p.Leu567Pro
CA16608769
NM_001348211.2:c.1700T>C