Canonical Allele Identifier: PA2828006367
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142268
ClinVar RCV Id: RCV000131289 RCV002228321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Val1321Ile
CA009548
NM_001354905.2:c.3961G>A