Canonical Allele Identifier: PA2827962648
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Val2640Ile
CA014160
NM_001354897.2:c.7918G>A