Canonical Allele Identifier: PA162197
Gene: SOCS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 135275
ClinVar RCV Id: RCV000122089 RCV000886018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003736.1:p.Gln210His
CA162196
NM_003745.2:c.630G>C
CA394739653
NM_003745.2:c.630G>T