Canonical Allele Identifier: PA2827950789
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 844658
ClinVar RCV Id: RCV003649314
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gly1037Val
CA16028028
NM_001354896.2:c.3110G>T