Canonical Allele Identifier: PA2828046922
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2082323
ClinVar RCV Id: RCV003534924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Met2238Val
CA046864
NM_001354904.2:c.6712A>G