Canonical Allele Identifier: PA16040135
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232420
ClinVar RCV Id: RCV000217741 RCV000987586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Leu2574Ile
CA10578449
NM_000038.6:c.7720C>A