Canonical Allele Identifier: PA2827986161
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142731

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Arg1409Gln
CA009471
NM_001354900.2:c.4226G>A