Canonical Allele Identifier: PA2827434815
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335149.1:p.Ala585Val
CA402528341
NM_001348220.1:c.1754C>T