Canonical Allele Identifier: PA2825842367
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1019337
ClinVar RCV Id: RCV001318759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135770.1:p.Ser265Thr
CA3600787
NM_001142298.2:c.793T>A