Canonical Allele Identifier: PA2827959793
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2874161
ClinVar RCV Id: RCV003743318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser1768Phe
CA16032859
NM_001354897.2:c.5303C>T