Canonical Allele Identifier: PA336779
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_001120982.1:p.Ile2615Val
CA336774
NM_001127510.3:c.7843A>G