Canonical Allele Identifier: PA2741902951
Gene: SOCS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2594005
ClinVar RCV Id: RCV004339989
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003868.1:p.Gly176Ser
CA6720058
NM_003877.5:c.526G>A