Canonical Allele Identifier: PA915996724
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 253029
ClinVar RCV Id: RCV000184066 RCV000652548 RCV001636735 RCV001155398 RCV002518539 RCV003387820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003891.1:p.Ala33Val
CA3600374
NM_003900.5:c.98C>T