Canonical Allele Identifier: PA2826319065
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 207529
ClinVar RCV Id: RCV000189717 RCV000560032
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230155.2:p.Ser204Asn
CA319094
NM_001243226.3:c.611G>A