Canonical Allele Identifier: PA916041490
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_001341825.1:p.Ile2533Val
CA013792
NM_001354896.2:c.7597A>G