Canonical Allele Identifier: PA916040466
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216168
ClinVar RCV Id: RCV000568323 RCV002247624 RCV002478702 RCV003765280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Glu1681Lys
CA040323
NM_001354896.2:c.5041G>A