Canonical Allele Identifier: PA319095
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 207529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077431.1:p.Ser102Asn
CA319094
NM_001083962.2:c.305G>A