Canonical Allele Identifier: PA2827980664
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133514
ClinVar RCV Id: RCV000120020 RCV000565915 RCV000589511 RCV003650377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ile2513Val
CA013946
NM_001354899.2:c.7537A>G