Canonical Allele Identifier: PA350690
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219535
ClinVar RCV Id: RCV000206690 RCV000235972 RCV000566249 RCV003997566 RCV000657022 RCV003534492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Val512Ala
CA028518
NM_001127511.3:c.1535T>C