Canonical Allele Identifier: PA2828049078
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_001341833.1:p.Ile2540Ser
CA16038704
NM_001354904.2:c.7619T>G