Canonical Allele Identifier: PA105140
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Tyr702His
CA273696
NM_005633.4:c.2104T>C