Canonical Allele Identifier: PA2827995500
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1483670
ClinVar RCV Id: RCV003773180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asp1473Glu
CA16031397
NM_001354901.2:c.4419C>A
CA16031398
NM_001354901.2:c.4419C>G