Canonical Allele Identifier: PA2828003859
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482344
ClinVar RCV Id: RCV000565897 RCV001253018 RCV002512116 RCV004000973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gly2234Asp
CA16036537
NM_001354902.2:c.6701G>A