Canonical Allele Identifier: PA2825023955
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2082323
ClinVar RCV Id: RCV003534924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Met2364Val
CA046864
NM_000038.6:c.7090A>G