Canonical Allele Identifier: PA891852170
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 576088

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Ile600Leu
CA45674350
NM_005633.4:c.1798A>C