Canonical Allele Identifier: PA2827989151
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2082323
ClinVar RCV Id: RCV003534924
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Met2323Val
CA046864
NM_001354900.2:c.6967A>G