Canonical Allele Identifier: PA2827998664
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487060
ClinVar RCV Id: RCV000565939 RCV003744577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2438Trp
CA16037624
NM_001354901.2:c.7313C>G