Canonical Allele Identifier: PA2828036443
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_001341833.1:p.Gly893Arg
CA16028023
NM_001354904.2:c.2677G>A
CA16028024
NM_001354904.2:c.2677G>C