Canonical Allele Identifier: PA2828343919
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 432062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356496.1:p.Ser253Arg
CA402701458
NM_001369567.1:c.759C>G
CA402701459
NM_001369567.1:c.759C>A
CA402701465
NM_001369567.1:c.757A>C