Canonical Allele Identifier: PA2828345038
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1722322
ClinVar RCV Id: RCV002302436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356498.1:p.Arg388Leu
CA402533894
NM_001369569.1:c.1163G>T