Canonical Allele Identifier: PA2827949995
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala449Val
CA16024253
NM_001354896.2:c.1346C>T