Canonical Allele Identifier: PA2825633502
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 926382
ClinVar RCV Id: RCV001188974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala1718Val
CA16032596
NM_001127510.3:c.5153C>T