Canonical Allele Identifier: PA2828893594
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Tyr695His
CA273696
NM_001382394.1:c.2083T>C