Canonical Allele Identifier: PA658689292
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 492672
ClinVar RCV Id: RCV000584585 RCV002404586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala2576Thr
CA16038108
NM_001127510.3:c.7726G>A