Canonical Allele Identifier: PA2825517489
Gene: TCF4 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077431.1:p.Pro657Ala
CA402527629
NM_001083962.2:c.1969C>G