Canonical Allele Identifier: PA2580298325
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1979648
ClinVar RCV Id: RCV002780055
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003891.1:p.Asp329Asn
CA362452362
NM_003900.5:c.985G>A