Canonical Allele Identifier: PA645387157
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 376542

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Asn233Tyr
CA16602968
NM_005633.4:c.697A>T