Canonical Allele Identifier: PA2827986902
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2775119
ClinVar RCV Id: RCV003585133
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ala1638Thr
CA16032343
NM_001354900.2:c.4912G>A