Canonical Allele Identifier: PA297942
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181826

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Lys2599Asn
CA014071
NM_001127510.3:c.7797A>C
CA16038265
NM_001127510.3:c.7797A>T