Canonical Allele Identifier: PA645401777
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 246324

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asn2220Asp
CA045646
NM_001127510.3:c.6658A>G