Canonical Allele Identifier: PA645399611
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411342
ClinVar RCV Id: RCV000473845 RCV000481597 RCV000779718 RCV000570317 RCV003743725 RCV004001915
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile1177Val
CA035626
NM_001127510.3:c.3529A>G