Canonical Allele Identifier: PA2827962390
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216179

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Lys2563Gln
CA338557
NM_001354897.2:c.7687A>C