Canonical Allele Identifier: PA2825638495
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 820019
ClinVar RCV Id: RCV001013037
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Leu571Ser
CA16025175
NM_001127511.3:c.1712T>C