Canonical Allele Identifier: PA645386981
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 373121

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.Arg225Gln
CA7177479
NM_006939.4:c.674G>A