Canonical Allele Identifier: PA2580298334
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_003891.1:p.Gln357His
CA362452736
NM_003900.5:c.1071G>C
CA362452739
NM_003900.5:c.1071G>T