Canonical Allele Identifier: PA156782
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133519
ClinVar RCV Id: RCV000120026 RCV000129039 RCV000198586 RCV000657042 RCV003534350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr1292Met
CA008722
NM_000038.6:c.3875C>T