Canonical Allele Identifier: PA2825021429
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 926382
ClinVar RCV Id: RCV001188974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala1718Val
CA16032596
NM_000038.6:c.5153C>T