Canonical Allele Identifier: PA2580337022
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2163082
ClinVar RCV Id: RCV003073112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.His306Arg
CA7177419
NM_006939.4:c.917A>G