Canonical Allele Identifier: PA2825024814
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 628605
ClinVar RCV Id: RCV000773146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.His2591Tyr
CA16038214
NM_000038.6:c.7771C>T