Canonical Allele Identifier: PA2828353785
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1600730
ClinVar RCV Id: RCV002124646
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356515.1:p.Pro634Ala
CA402527629
NM_001369586.1:c.1900C>G