Canonical Allele Identifier: PA916040462
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 632641
ClinVar RCV Id: RCV000779740 RCV003584740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser1676Thr
CA16032217
NM_001354896.2:c.5027G>C