Canonical Allele Identifier: PA2828007677
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1730350
ClinVar RCV Id: RCV002326526
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr1021Lys
CA16028645
NM_001354902.2:c.3062C>A