Canonical Allele Identifier: PA2827992190
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41518
ClinVar RCV Id: RCV000034403 RCV000472427 RCV000564391 RCV000780856 RCV002228091 RCV003996158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Arg440Gly
CA005217
NM_001354901.2:c.1318C>G