Canonical Allele Identifier: PA156732
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133510
ClinVar RCV Id: RCV000120015 RCV000122777 RCV000148358 RCV000589855 RCV000131786 RCV003764834 RCV003915187
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Met1413Val
CA009368
NM_000038.6:c.4237A>G