Canonical Allele Identifier: PA2828030169
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927745
ClinVar RCV Id: RCV001191231 RCV003538596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ala2629Ser
CA16039107
NM_001354903.2:c.7885G>T