Canonical Allele Identifier: PA1139741873
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 859980
ClinVar RCV Id: RCV002462315 RCV002411592 RCV003537459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gln2618Glu
CA16038267
NM_001354896.2:c.7852C>G