Canonical Allele Identifier: PA2828009136
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1014518
ClinVar RCV Id: RCV003770651

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro1493Ala
CA16031748
NM_001354902.2:c.4477C>G