Canonical Allele Identifier: PA2828019003
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 934037
ClinVar RCV Id: RCV003650659
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Gly918Arg
CA16028023
NM_001354903.2:c.2752G>A
CA16028024
NM_001354903.2:c.2752G>C