Canonical Allele Identifier: PA2499252148
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1064027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn2636Ile
CA16038397
NM_001354896.2:c.7907A>T