Canonical Allele Identifier: PA297239
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.His1175Pro
CA297237
NM_005633.4:c.3524A>C