Canonical Allele Identifier: PA916047850
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 207529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356515.1:p.Ser78Asn
CA319094
NM_001369586.1:c.233G>A