Canonical Allele Identifier: PA2828894671
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40686

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Leu569Val
CA1624560
NM_001382395.1:c.1705C>G