Canonical Allele Identifier: PA658659333
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482340
ClinVar RCV Id: RCV000563785 RCV002526856 RCV003652002 RCV004000972
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asn660Ser
CA16025642
NM_001127510.3:c.1979A>G