Canonical Allele Identifier: PA2828346333
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 207529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356501.1:p.Ser102Asn
CA319094
NM_001369572.1:c.305G>A