Canonical Allele Identifier: PA2828895149
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40733
ClinVar Variation Id: 45365

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Asp1185Glu
CA136143
NM_001382395.1:c.3555C>A
CA297240
NM_001382395.1:c.3555C>G