Canonical Allele Identifier: PA2827986601
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1003903
ClinVar RCV Id: RCV002242020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ala1541Val
CA16031739
NM_001354900.2:c.4622C>T