Canonical Allele Identifier: PA2829450600
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_003891.1:p.Arg110His
CA362443434
NM_003900.5:c.329G>A