Canonical Allele Identifier: PA1139741885
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 923839
ClinVar RCV Id: RCV001184856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ile2633Arg
CA16038375
NM_001354896.2:c.7898T>G