Canonical Allele Identifier: PA891859046
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 566965
ClinVar RCV Id: RCV003534567
ClinVar Variation Id: 1770531
ClinVar RCV Id: RCV002387879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Val450Leu
CA16024255
NM_001127510.3:c.1348G>C
CA16024256
NM_001127510.3:c.1348G>T