Canonical Allele Identifier: PA2827433814
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335147.1:p.Ala590Val
CA402528341
NM_001348218.2:c.1769C>T