Canonical Allele Identifier: PA215469
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41507
ClinVar RCV Id: RCV000034391
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Leu1706Val
CA009899
NM_001127511.3:c.5116C>G