Canonical Allele Identifier: PA2828018691
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469780
ClinVar RCV Id: RCV000579991 RCV001357578 RCV003742628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser869Asn
CA033901
NM_001354903.2:c.2606G>A