Canonical Allele Identifier: PA2827990109
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3069477
ClinVar RCV Id: RCV004008021
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Val2610Ile
CA16038596
NM_001354900.2:c.7828G>A