Canonical Allele Identifier: PA2826916107
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2119883
ClinVar RCV Id: RCV003024873

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293136.1:p.Gly343Arg
CA402534328
NM_001306207.1:c.1027G>A
CA402534330
NM_001306207.1:c.1027G>C