Canonical Allele Identifier: PA2827980742
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2566987
ClinVar RCV Id: RCV003278281
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Trp2536Gly
CA16038033
NM_001354899.2:c.7606T>G