Canonical Allele Identifier: PA2580298331
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1943712
ClinVar RCV Id: RCV002662987
ClinVar Variation Id: 2923831
ClinVar RCV Id: RCV003783389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003891.1:p.Gln354His
CA133109719
NM_003900.5:c.1062G>C
CA362452695
NM_003900.5:c.1062G>T