Canonical Allele Identifier: PA2825641513
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1369536
ClinVar RCV Id: RCV001870683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr1567Ala
CA16031754
NM_001127511.3:c.4699A>G