Canonical Allele Identifier: PA2828012080
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Met2400Val
CA048161
NM_001354902.2:c.7198A>G