Canonical Allele Identifier: PA2828893522
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 944819
ClinVar RCV Id: RCV001215308

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Ile603Val
CA1624545
NM_001382394.1:c.1807A>G