Canonical Allele Identifier: PA2827987695
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127308
ClinVar RCV Id: RCV000115106 RCV000562980 RCV003153365 RCV003997224 RCV002228239 RCV003474709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Arg1879Gly
CA010637
NM_001354900.2:c.5635C>G