Canonical Allele Identifier: PA2827950806
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1727262
ClinVar RCV Id: RCV002319777 RCV002463198 RCV003743933
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro1042Leu
CA16028060
NM_001354896.2:c.3125C>T