Canonical Allele Identifier: PA16039837
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230838
ClinVar RCV Id: RCV000217057 RCV000585258 RCV002494587 RCV003475011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gln445Glu
CA10578313
NM_000038.6:c.1333C>G