Canonical Allele Identifier: PA2828007606
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1428375
ClinVar RCV Id: RCV001936278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asp1562His
CA16032618
NM_001354905.2:c.4684G>C