Canonical Allele Identifier: PA2827986971
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 234162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ala1659Val
CA10578393
NM_001354900.2:c.4976C>T