Canonical Allele Identifier: PA2826916538
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1801341
ClinVar RCV Id: RCV002463402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293137.1:p.Ala298Thr
CA8970270
NM_001306208.1:c.892G>A