Canonical Allele Identifier: PA916041489
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411403
ClinVar RCV Id: RCV000575061 RCV001778967 RCV001764443 RCV002523368 RCV003409635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr2532Ala
CA048361
NM_001354896.2:c.7594A>G