Canonical Allele Identifier: PA2827966863
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2054609
ClinVar RCV Id: RCV003744812
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp1113Asn
CA16028812
NM_001354898.2:c.3337G>A