Canonical Allele Identifier: PA2741903423
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2926556
ClinVar RCV Id: RCV003788794
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003891.1:p.Pro384Ala
CA362453086
NM_003900.5:c.1150C>G