Canonical Allele Identifier: PA156747
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133513
ClinVar RCV Id: RCV000167973 RCV000120019 RCV000572762 RCV001527676 RCV003315714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ile2515Val
CA013792
NM_000038.6:c.7543A>G