Canonical Allele Identifier: PA104856
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40673

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Cys441Tyr
CA273441
NM_005633.4:c.1322G>A