Canonical Allele Identifier: PA2573229769
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1690409
ClinVar RCV Id: RCV002252827
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003891.1:p.Asp335Glu
CA362452441
NM_003900.5:c.1005T>A
CA362452442
NM_003900.5:c.1005T>G