Canonical Allele Identifier: PA2827946961
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_001341824.1:p.Gly2325Asp
CA16036537
NM_001354895.2:c.6974G>A