Canonical Allele Identifier: PA2828032499
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 234001

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro322Ala
CA027206
NM_001354904.2:c.964C>G