Canonical Allele Identifier: PA2827951172
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181801

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Lys1157Gln
CA008372
NM_001354896.2:c.3469A>C