Canonical Allele Identifier: PA2828347788
Gene: TCF4 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356503.1:p.Pro652Ala
CA402527629
NM_001369574.1:c.1954C>G