Canonical Allele Identifier: PA658810298
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 517435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Ile1287Val
CA1624103
NM_005633.4:c.3859A>G