Canonical Allele Identifier: PA1139736611
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 926362
ClinVar RCV Id: RCV001188921 RCV002560936
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Leu647Ser
CA16025442
NM_001354896.2:c.1940T>C