Canonical Allele Identifier: PA16040122
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Met2491Val
CA048161
NM_000038.6:c.7471A>G