Canonical Allele Identifier: PA2828348731
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 93542

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356505.1:p.Arg553His
CA266820
NM_001369576.1:c.1658G>A