Canonical Allele Identifier: PA2827982954
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ala390Val
CA16024253
NM_001354900.2:c.1169C>T