Canonical Allele Identifier: PA2826320395
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 207529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230159.1:p.Ser100Asn
CA319094
NM_001243230.2:c.299G>A