Canonical Allele Identifier: PA2827968993
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2789833
ClinVar RCV Id: RCV003745773

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro1753Ser
CA16032989
NM_001354898.2:c.5257C>T