Allele Registry

Canonical Allele Identifier: PA915996815

Gene: SQSTM1 HGNC NCBI

ClinVar Variation Id: 650222

HGVS (amino-acid)	Matching Registered Transcripts
NP_003891.1:p.Asp329Gly	CA3600776 NM_003900.5:c.986A>G