Canonical Allele Identifier: PA2828352805
Gene: TCF4 HGNC NCBI
ClinVar RCV:
RCV002124646
ClinVar Variation:
1600730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356513.1:p.Pro628Ala
CA402527629
NM_001369584.1:c.1882C>G