Canonical Allele Identifier: PA2828352869
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_001356514.1:p.Ser78Asn
CA319094
NM_001369585.1:c.233G>A