Canonical Allele Identifier: PA2827335487
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2699156
ClinVar RCV Id: RCV003507653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317533.1:p.Leu578Pro
CA402528906
NM_001330604.3:c.1733T>C