Canonical Allele Identifier: PA2825641770
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 655278
ClinVar RCV Id: RCV001805886 RCV003536007
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Glu1655Gly
CA16032310
NM_001127511.3:c.4964A>G