Canonical Allele Identifier: PA2825635701
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1757329
ClinVar RCV Id: RCV002367475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr2379Asn
CA16036873
NM_001127510.3:c.7136C>A