Canonical Allele Identifier: PA2828022586
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141684
ClinVar RCV Id: RCV000130298 RCV003534380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ile1478Val
CA009718
NM_001354903.2:c.4432A>G