Canonical Allele Identifier: PA2828013058
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1064027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn2458Ile
CA16038397
NM_001354905.2:c.7373A>T