Canonical Allele Identifier: PA2828353306
Gene: TCF4 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356514.1:p.Pro628Ala
CA402527629
NM_001369585.1:c.1882C>G