Canonical Allele Identifier: PA156837
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133528
ClinVar RCV Id: RCV000120038 RCV000767181 RCV002453438 RCV003534352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gly1109Cys
CA008272
NM_000038.6:c.3325G>T