Canonical Allele Identifier: PA2828353752
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 393171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356515.1:p.Leu586Pro
CA16608769
NM_001369586.1:c.1757T>C