Canonical Allele Identifier: PA1139733723
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537689
ClinVar RCV Id: RCV003534539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg45Pro
CA124925217
NM_001354902.2:c.134G>C