Canonical Allele Identifier: PA1139739890
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 949496
ClinVar RCV Id: RCV002241284
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser1772Cys
CA16032837
NM_001354896.2:c.5315C>G