Canonical Allele Identifier: PA2827433339
Gene: TCF4 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001335146.1:p.Pro633Ala
CA402527629
NM_001348217.1:c.1897C>G