Canonical Allele Identifier: PA916039691
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469722
ClinVar RCV Id: RCV000564731 RCV003743782
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp669Gly
CA16025584
NM_001354896.2:c.2006A>G