Canonical Allele Identifier: PA2827960826
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489476
ClinVar RCV Id: RCV000579432 RCV001800796 RCV003537232
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp2089Ala
CA044147
NM_001354897.2:c.6266A>C