Canonical Allele Identifier: PA645398831
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411351
ClinVar RCV Id: RCV001017272 RCV002469156 RCV004001917 RCV003651841
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asp366Asn
CA026688
NM_001127510.3:c.1096G>A