Canonical Allele Identifier: PA2825842385
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1943712
ClinVar RCV Id: RCV002662987
ClinVar Variation Id: 2923831
ClinVar RCV Id: RCV003783389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135770.1:p.Gln270His
CA133109719
NM_001142298.2:c.810G>C
CA362452695
NM_001142298.2:c.810G>T