Canonical Allele Identifier: PA2827947912
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1064027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asn2618Ile
CA16038397
NM_001354895.2:c.7853A>T