Canonical Allele Identifier: PA2827432837
Gene: TCF4 HGNC NCBI
ClinVar RCV:
RCV002124646
ClinVar Variation:
1600730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335145.1:p.Pro497Ala
CA402527629
NM_001348216.2:c.1489C>G