Canonical Allele Identifier: PA2825018278
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537413
ClinVar RCV Id: RCV002234011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gly1039Leu
CA658796577
NM_000038.6:c.3115_3116delinsCT