Canonical Allele Identifier: PA2741934054
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3039811
ClinVar RCV Id: RCV003931827
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.Phe290Leu
CA389647120
NM_006939.4:c.870T>G
CA389647121
NM_006939.4:c.870T>A
CA389647126
NM_006939.4:c.868T>C