Canonical Allele Identifier: PA2827999067
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 75619
ClinVar RCV Id: RCV000662519 RCV003650363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro2563Leu
CA16038424
NM_001354901.2:c.7688C>T