Canonical Allele Identifier: PA916041714
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537538
ClinVar RCV Id: RCV003538504
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr2733Ala
CA16039014
NM_001354896.2:c.8197A>G