Canonical Allele Identifier: PA190117
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41513
ClinVar RCV Id: RCV000034398 RCV000122799 RCV000164132 RCV000235447 RCV000408370 RCV002228086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala2472Val
CA013674
NM_001127510.3:c.7415C>T