Canonical Allele Identifier: PA2828001366
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 934537
ClinVar RCV Id: RCV003650661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala920Glu
CA16027964
NM_001354902.2:c.2759C>A