Canonical Allele Identifier: PA2828006141
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_001341834.1:p.Met1253Val
CA009368
NM_001354905.2:c.3757A>G