Canonical Allele Identifier: PA2827977936
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1745553
ClinVar RCV Id: RCV002344228
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro1683Thr
CA16032543
NM_001354899.2:c.5047C>A