Canonical Allele Identifier: PA2828895199
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 45369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Gly1230Val
CA136155
NM_001382395.1:c.3689G>T