Canonical Allele Identifier: PA916040496
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411515
ClinVar RCV Id: RCV000482697 RCV000580947 RCV001293489 RCV003392285 RCV004001970 RCV003651883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg1705Gln
CA040507
NM_001354896.2:c.5114G>A