Canonical Allele Identifier: PA658660009
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482322
ClinVar RCV Id: RCV000574030 RCV003537129
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro1542Arg
CA16031465
NM_001127510.3:c.4625C>G