Canonical Allele Identifier: PA915978450
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 202212
ClinVar RCV Id: RCV000254519 RCV000873998 RCV001157082 RCV001579939
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135771.1:p.Ala33Val
CA346905
NM_001142299.2:c.98C>T