Canonical Allele Identifier: PA915996844
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 648242
ClinVar RCV Id: RCV000802926

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003891.1:p.Ser366Cys
CA362452895
NM_003900.5:c.1097C>G