Canonical Allele Identifier: PA2827957302
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1042543
ClinVar RCV Id: RCV002242366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp1028Tyr
CA16028017
NM_001354897.2:c.3082G>T