Canonical Allele Identifier: PA2825018266
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 822908
ClinVar RCV Id: RCV001018671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Leu1036Trp
CA16028141
NM_000038.6:c.3107T>G