Canonical Allele Identifier: PA2827972071
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 957959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Met2688Val
CA16039002
NM_001354898.2:c.8062A>G