Canonical Allele Identifier: PA2827996701
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236622
ClinVar RCV Id: RCV000229356 RCV000506645 RCV000569562 RCV003650531 RCV003998677
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn1844Ser
CA042707
NM_001354901.2:c.5531A>G