Canonical Allele Identifier: PA2826321739
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230161.1:p.Ala543Val
CA402528341
NM_001243232.1:c.1628C>T