Canonical Allele Identifier: PA2828015361
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ala166Val
CA16024253
NM_001354906.2:c.497C>T