Canonical Allele Identifier: PA2827985117
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181801

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Lys1098Gln
CA008372
NM_001354900.2:c.3292A>C