Canonical Allele Identifier: PA2828347253
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356502.1:p.Ala609Val
CA402528341
NM_001369573.1:c.1826C>T