Canonical Allele Identifier: PA645398886
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Met466Val
CA027319
NM_001127510.3:c.1396A>G