Canonical Allele Identifier: PA2828016619
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_001341835.1:p.Asn377Ser
CA16025642
NM_001354906.2:c.1130A>G