Canonical Allele Identifier: PA2827961800
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1359860
ClinVar RCV Id: RCV003772508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gln2385Pro
CA16036847
NM_001354897.2:c.7154A>C