Canonical Allele Identifier: PA2826321705
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 93542

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230161.1:p.Arg507His
CA266820
NM_001243232.1:c.1520G>A