Canonical Allele Identifier: PA297269
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40674

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Phe462Tyr
CA297267
NM_005633.4:c.1385T>A