Canonical Allele Identifier: PA2828346261
Gene: TCF4 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356500.1:p.Pro653Ala
CA402527629
NM_001369571.1:c.1957C>G