Canonical Allele Identifier: PA2828037388
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181801

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Lys1013Gln
CA008372
NM_001354904.2:c.3037A>C