Canonical Allele Identifier: PA916042651
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411340
ClinVar RCV Id: RCV000575397 RCV001591101 RCV003766554 RCV004001914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Gln910Arg
CA16029193
NM_001354906.2:c.2729A>G