Canonical Allele Identifier: PA2827430668
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 432062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335140.1:p.Ser211Arg
CA402701458
NM_001348211.2:c.633C>G
CA402701459
NM_001348211.2:c.633C>A
CA402701465
NM_001348211.2:c.631A>C