Canonical Allele Identifier: PA916039937
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219437
ClinVar RCV Id: RCV000204328 RCV000478187 RCV000565056 RCV003491951 RCV003650460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser899Phe
CA348575
NM_001354896.2:c.2696C>T