Canonical Allele Identifier: PA2825018128
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Met1014Val
CA16027984
NM_000038.6:c.3040A>G