Canonical Allele Identifier: PA2825842463
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2577014
ClinVar RCV Id: RCV003323343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135770.1:p.Pro303Ala
CA3600812
NM_001142298.2:c.907C>G