Canonical Allele Identifier: PA2828016527
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 439412
ClinVar RCV Id: RCV000507769
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ile363Arg
CA16025550
NM_001354906.2:c.1088T>G