Canonical Allele Identifier: PA297798
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181798
ClinVar RCV Id: RCV000159546 RCV000218802 RCV003743595
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ile1007Val
CA008024
NM_001127511.3:c.3019A>G