Canonical Allele Identifier: PA297198
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40734

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Asp1243Glu
CA297196
NM_005633.4:c.3729C>G
CA346362436
NM_005633.4:c.3729C>A