Canonical Allele Identifier: PA2828348792
Gene: TCF4 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356505.1:p.Pro632Ala
CA402527629
NM_001369576.1:c.1894C>G