Canonical Allele Identifier: PA297814
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181801

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Lys1139Gln
CA008372
NM_000038.6:c.3415A>C