Canonical Allele Identifier: PA2828048758
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1064027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn2492Ile
CA16038397
NM_001354904.2:c.7475A>T