Canonical Allele Identifier: PA2828007440
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1331902
ClinVar RCV Id: RCV001804418
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Thr1537Ser
CA16032458
NM_001354905.2:c.4609A>T