Canonical Allele Identifier: PA2828009746
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2789833
ClinVar RCV Id: RCV003745773

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro1687Ser
CA16032989
NM_001354902.2:c.5059C>T