Canonical Allele Identifier: PA2827983527
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1399922
ClinVar RCV Id: RCV001925034
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Val601Met
CA029894
NM_001354900.2:c.1801G>A