Canonical Allele Identifier: PA2827979030
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411334
ClinVar RCV Id: RCV000571749 RCV000733231 RCV003651838 RCV004001912
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2016Asn
CA043925
NM_001354899.2:c.6047G>A