Canonical Allele Identifier: PA2828002832
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1745920
ClinVar RCV Id: RCV002338512
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala1640Ser
CA16032678
NM_001354902.2:c.4918G>T