Canonical Allele Identifier: PA2828345301
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1791142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356499.1:p.Thr81Ser
CA8970612
NM_001369570.1:c.242C>G
CA402703575
NM_001369570.1:c.241A>T