Canonical Allele Identifier: PA2827989007
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232817
ClinVar RCV Id: RCV000215442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Leu2276Ser
CA046501
NM_001354900.2:c.6827T>C