Canonical Allele Identifier: PA2826319065
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 207529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230155.2:p.Ser204Asn
CA319094
NM_001243226.3:c.611G>A