Canonical Allele Identifier: PA2828345216
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356498.1:p.Ala613Val
CA402528341
NM_001369569.1:c.1838C>T