Canonical Allele Identifier: PA2826320880
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_001230160.1:p.Ser60Asn
CA319094
NM_001243231.2:c.179G>A