Canonical Allele Identifier: PA2828347755
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 393171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356503.1:p.Leu604Pro
CA16608769
NM_001369574.1:c.1811T>C