Canonical Allele Identifier: PA2825842819
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2931971
ClinVar RCV Id: RCV003792993
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135771.1:p.Asn246Asp
CA362452379
NM_001142299.2:c.736A>G