Canonical Allele Identifier: PA2827968697
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1745225
ClinVar RCV Id: RCV002335894
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gly1669Asp
CA16032440
NM_001354898.2:c.5006G>A