Canonical Allele Identifier: PA2573229773
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1498798
ClinVar RCV Id: RCV002003978
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003891.1:p.Gln357Glu
CA362452727
NM_003900.5:c.1069C>G