Canonical Allele Identifier: PA2827963639
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411467
ClinVar RCV Id: RCV002248689 RCV003651870
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Val99Ile
CA16022128
NM_001354898.2:c.295G>A