Canonical Allele Identifier: PA2827999077
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 949059
ClinVar RCV Id: RCV003650741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2566Asn
CA16038441
NM_001354901.2:c.7697G>A