Canonical Allele Identifier: PA658700828
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 496306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Ser1242Gly
CA346362449
NM_005633.4:c.3724A>G