Canonical Allele Identifier: PA2828347730
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 7370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356503.1:p.Arg575Trp
CA254160
NM_001369574.1:c.1723C>T