Canonical Allele Identifier: PA913200206
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629986
ClinVar RCV Id: RCV000774851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asp1134Gly
CA16028788
NM_001127510.3:c.3401A>G