Canonical Allele Identifier: PA2828347761
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356503.1:p.Ala609Val
CA402528341
NM_001369574.1:c.1826C>T