Canonical Allele Identifier: PA645386985
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 373114
ClinVar RCV Id: RCV000414175 RCV001250768
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.Met267Thr
CA16021010
NM_006939.4:c.800T>C