Canonical Allele Identifier: PA2828009751
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3230729
ClinVar RCV Id: RCV004522844
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro1687His
CA16032990
NM_001354902.2:c.5060C>A