Canonical Allele Identifier: PA2827981041
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761409
ClinVar RCV Id: RCV002416908
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Glu2627Gly
CA16038626
NM_001354899.2:c.7880A>G