Canonical Allele Identifier: PA2828021702
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142731

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Arg1349Gln
CA009471
NM_001354903.2:c.4046G>A