Canonical Allele Identifier: PA2828042273
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ile1564Val
CA040590
NM_001354904.2:c.4690A>G