Canonical Allele Identifier: PA163879
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135695
ClinVar RCV Id: RCV000122769 RCV000129141 RCV000200967 RCV000210128 RCV000589216 RCV003743578 RCV003315800 RCV003905172 RCV001353757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Arg99Trp
CA007948
NM_000038.6:c.295C>T