Canonical Allele Identifier: PA2827954279
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133505
ClinVar RCV Id: RCV000120009 RCV000123676 RCV000238598 RCV000410035 RCV003103728
ClinVar Variation Id: 1056172
ClinVar RCV Id: RCV002242581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser26Arg
CA025425
NM_001354897.2:c.78C>A
CA360611868
NM_001354897.2:c.76A>C
CA360611883
NM_001354897.2:c.78C>G