Canonical Allele Identifier: PA2827992699
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236567
ClinVar RCV Id: RCV000679050 RCV000574116 RCV002267974 RCV002516262 RCV003535601 RCV003998658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ile617Val
CA030596
NM_001354901.2:c.1849A>G