Canonical Allele Identifier: PA2828002905
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411404

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ile1688Met
CA041612
NM_001354902.2:c.5064A>G