Canonical Allele Identifier: PA2827977847
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411515

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Arg1659Gln
CA040507
NM_001354899.2:c.4976G>A