Allele Registry

Canonical Allele Identifier: PA2825842120

Gene: SQSTM1 HGNC NCBI

ClinVar Allele:

455004

ClinVar RCV:

RCV000544306

ClinVar Variation:

475404

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135770.1:p.Val171Leu	CA3600669 NM_001142298.2:c.511G>C