Canonical Allele Identifier: PA645387031
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 421233

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.Ala1195Val
CA7176746
NM_006939.4:c.3584C>T