Canonical Allele Identifier: PA2827962764
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3075238
ClinVar RCV Id: RCV004015764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ile2676Ser
CA16038704
NM_001354897.2:c.8027T>G