Canonical Allele Identifier: PA2828348290
Gene: TCF4 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356504.1:p.Pro633Ala
CA402527629
NM_001369575.1:c.1897C>G