Canonical Allele Identifier: PA2826320027
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 432062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230157.1:p.Ser259Arg
CA402701458
NM_001243228.2:c.777C>G
CA402701459
NM_001243228.2:c.777C>A
CA402701465
NM_001243228.2:c.775A>C