Canonical Allele Identifier: PA2826321732
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 393171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230161.1:p.Leu538Pro
CA16608769
NM_001243232.1:c.1613T>C