Canonical Allele Identifier: PA2825842375
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3169799
ClinVar RCV Id: RCV004458157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135770.1:p.Glu268Val
CA362452646
NM_001142298.2:c.803A>T