Canonical Allele Identifier: PA2827999043
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216180
ClinVar RCV Id: RCV000196896 RCV000574010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ile2556Val
CA336774
NM_001354901.2:c.7666A>G