Canonical Allele Identifier: PA2827992660
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232098
ClinVar RCV Id: RCV000214596 RCV000474515 RCV000483692 RCV000677741 RCV000657144 RCV000677742 RCV003650490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Leu603Ile
CA030573
NM_001354901.2:c.1807C>A