Canonical Allele Identifier: PA2827950699
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411386
ClinVar RCV Id: RCV000561099 RCV000758725 RCV004001931 RCV003651848 RCV002526443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp1007Gly
CA034127
NM_001354896.2:c.3020A>G