Canonical Allele Identifier: PA2827942601
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 970107
ClinVar RCV Id: RCV003652102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asp1015Gly
CA16027996
NM_001354895.2:c.3044A>G