Canonical Allele Identifier: PA2827981241
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 957959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Met2685Val
CA16039002
NM_001354899.2:c.8053A>G