Canonical Allele Identifier: PA2827966752
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1730223
ClinVar RCV Id: RCV002326403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn1083Ile
CA16028622
NM_001354898.2:c.3248A>T