Canonical Allele Identifier: PA2825014988
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1316460
ClinVar RCV Id: RCV001774832 RCV003772073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ile446Leu
CA16024229
NM_000038.6:c.1336A>C