Canonical Allele Identifier: PA2827996201
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ile1687Val
CA009948
NM_001354901.2:c.5059A>G