Canonical Allele Identifier: PA2826916689
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 381549
ClinVar RCV Id: RCV000431775 RCV000623167 RCV001507071 RCV003422397
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001293137.1:p.Arg501Gln
CA16607615
NM_001306208.1:c.1502G>A