Canonical Allele Identifier: PA2825841782
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1057481
ClinVar RCV Id: RCV001366472 RCV002290695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135770.1:p.Lys19Arg
CA3600462
NM_001142298.2:c.56A>G