Canonical Allele Identifier: PA2828023748
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1746238
ClinVar RCV Id: RCV002344319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Lys1643Thr
CA16032764
NM_001354903.2:c.4928A>C