Canonical Allele Identifier: PA2826519921
Gene: SOCS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2594005
ClinVar RCV Id: RCV004339989
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001257398.1:p.Gly176Ser
CA6720058
NM_001270469.2:c.526G>A