Canonical Allele Identifier: PA916042002
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233215
ClinVar RCV Id: RCV000213818 RCV001800574 RCV002515704 RCV003743671
ClinVar Variation Id: 862543
ClinVar RCV Id: RCV001200168 RCV002554571 RCV003650592
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser987Arg
CA10578350
NM_001354900.2:c.2961T>A
CA16028081
NM_001354900.2:c.2959A>C
CA16028087
NM_001354900.2:c.2961T>G