Canonical Allele Identifier: PA203869
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 202211
ClinVar RCV Id: RCV000184065 RCV000481808 RCV001323701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135770.1:p.Pro303Leu
CA203868
NM_001142298.2:c.908C>T