Canonical Allele Identifier: PA2826322944
Gene: TCF4 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230164.1:p.Pro493Ala
CA402527629
NM_001243235.2:c.1477C>G