Canonical Allele Identifier: PA913200287
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 630006
ClinVar RCV Id: RCV000774872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gly1674Ala
CA16032318
NM_001127510.3:c.5021G>C