Canonical Allele Identifier: PA2825842391
Gene: SQSTM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2157881
ClinVar RCV Id: RCV003079693
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135770.1:p.Gln273His
CA362452736
NM_001142298.2:c.819G>C
CA362452739
NM_001142298.2:c.819G>T