Canonical Allele Identifier: PA2825842880
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1352802
ClinVar RCV Id: RCV002039963 RCV003334056 RCV004529028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135771.1:p.Ala296Val
CA362453044
NM_001142299.2:c.887C>T