Canonical Allele Identifier: PA2828346743
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356501.1:p.Ala610Val
CA402528341
NM_001369572.1:c.1829C>T