Canonical Allele Identifier: PA2825644693
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1064027

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asn2600Ile
CA16038397
NM_001127511.3:c.7799A>T