Canonical Allele Identifier: PA891861069
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 581714
ClinVar RCV Id: RCV000705624 RCV001561077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077431.1:p.Ala614Val
CA402528341
NM_001083962.2:c.1841C>T