Canonical Allele Identifier: PA2828002391
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_001341831.1:p.Asp1441Glu
CA16031397
NM_001354902.2:c.4323C>A
CA16031398
NM_001354902.2:c.4323C>G