Canonical Allele Identifier: PA2499275418
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1022639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.His1301Arg
CA7176691
NM_006939.4:c.3902A>G