Canonical Allele Identifier: PA2825842888
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2926556
ClinVar RCV Id: RCV003788794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135771.1:p.Pro300Ala
CA362453086
NM_001142299.2:c.898C>G