Canonical Allele Identifier: PA2828009130
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 640694
ClinVar RCV Id: RCV002334472 RCV003744657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Met1492Val
CA039697
NM_001354902.2:c.4474A>G