Canonical Allele Identifier: PA2825025119
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_000029.2:p.Ile2666Ser
CA16038704
NM_000038.6:c.7997T>G