Canonical Allele Identifier: PA2827999636
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141047
ClinVar RCV Id: RCV000129383 RCV000148362 RCV000235766 RCV000410318 RCV000657075 RCV003315875
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ala2736Thr
CA015437
NM_001354901.2:c.8206G>A