Canonical Allele Identifier: PA645399802
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231488
ClinVar RCV Id: RCV000223153 RCV003534519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile1311Ser
CA10578361
NM_001127510.3:c.3932T>G