Canonical Allele Identifier: PA2828352304
Gene: TCF4 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356512.1:p.Pro629Ala
CA402527629
NM_001369583.1:c.1885C>G