Canonical Allele Identifier: PA2827971967
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1317229
ClinVar RCV Id: RCV001759101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ile2658Ser
CA16038805
NM_001354898.2:c.7973T>G