Canonical Allele Identifier: PA162193
Gene: SOCS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 135273
ClinVar RCV Id: RCV000122087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003736.1:p.Gln6Glu
CA162192
NM_003745.2:c.16C>G