Canonical Allele Identifier: PA2741837529
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2634117
ClinVar RCV Id: RCV003778279 RCV004531669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135771.1:p.Arg26His
CA362443434
NM_001142299.2:c.77G>A