Canonical Allele Identifier: PA156757
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133515
ClinVar RCV Id: RCV000120021 RCV000222148 RCV000767111 RCV000409341 RCV003997328 RCV003315715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Glu2758Gly
CA014512
NM_000038.6:c.8273A>G