Canonical Allele Identifier: PA2825842868
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 448529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135771.1:p.Ser286Pro
CA3600800
NM_001142299.2:c.856T>C