Canonical Allele Identifier: PA2825842829
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_001135771.1:p.Asp251Glu
CA362452441
NM_001142299.2:c.753T>A
CA362452442
NM_001142299.2:c.753T>G