Canonical Allele Identifier: PA2827967383
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_001341827.1:p.Thr1267Met
CA008722
NM_001354898.2:c.3800C>T