Canonical Allele Identifier: PA2827943607
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 822

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ile1307Lys
CA008761
NM_001354895.2:c.3920T>A