Canonical Allele Identifier: PA16040108
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236641
ClinVar RCV Id: RCV001026077 RCV003535639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr2379Ile
CA10582339
NM_000038.6:c.7136C>T