Canonical Allele Identifier: PA2827998777
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220176
ClinVar RCV Id: RCV000203815 RCV000561106 RCV000587117 RCV001002346 RCV003316138 RCV003997620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.His2473Tyr
CA048637
NM_001354901.2:c.7417C>T