Canonical Allele Identifier: PA2827431752
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335142.1:p.Ala484Val
CA402528341
NM_001348213.2:c.1451C>T