Canonical Allele Identifier: PA2828001377
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482459
ClinVar RCV Id: RCV000570784 RCV003537164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asp925Val
CA16028005
NM_001354902.2:c.2774A>T