Canonical Allele Identifier: PA2828349796
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1600730
ClinVar RCV Id: RCV002124646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356507.1:p.Pro632Ala
CA402527629
NM_001369578.1:c.1894C>G