Canonical Allele Identifier: PA645400659
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 422390
ClinVar RCV Id: RCV000485630 RCV002350071 RCV003535762 RCV002248706 RCV004003374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asn1908Ser
CA16033859
NM_001127510.3:c.5723A>G