Canonical Allele Identifier: PA645449886
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 393171
ClinVar RCV Id: RCV000418798 RCV001507045
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077431.1:p.Leu609Pro
CA16608769
NM_001083962.2:c.1826T>C