Canonical Allele Identifier: PA2825842402
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2953215
ClinVar RCV Id: RCV003810333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135770.1:p.Ser277Ala
CA362452801
NM_001142298.2:c.829T>G