Canonical Allele Identifier: PA2499252414
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1000532
ClinVar RCV Id: RCV003770498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Val17Ile
CA360611763
NM_001354902.2:c.49G>A