Canonical Allele Identifier: PA2825023986
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Met2373Arg
CA16036833
NM_000038.6:c.7118T>G