Canonical Allele Identifier: PA2827978099
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1716320
ClinVar RCV Id: RCV003743856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser1729Phe
CA16032853
NM_001354899.2:c.5186C>T