Canonical Allele Identifier: PA2828352084
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2119883
ClinVar RCV Id: RCV003024873
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356512.1:p.Gly343Arg
CA402534328
NM_001369583.1:c.1027G>A
CA402534330
NM_001369583.1:c.1027G>C