Canonical Allele Identifier: PA105008
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Met269Thr
CA235344
NM_005633.4:c.806T>C