Canonical Allele Identifier: PA2827431936
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2119883
ClinVar RCV Id: RCV003024873
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335143.1:p.Gly206Arg
CA402534328
NM_001348214.2:c.616G>A
CA402534330
NM_001348214.2:c.616G>C