Canonical Allele Identifier: PA2828352039
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2240625
ClinVar RCV Id: RCV002719286
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356512.1:p.Ser281Gly
CA402701102
NM_001369583.1:c.841A>G