Canonical Allele Identifier: PA2828894781
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 191107

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Tyr702Cys
CA236034
NM_001382395.1:c.2105A>G