Canonical Allele Identifier: PA2828893512
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1369301
ClinVar RCV Id: RCV001874630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Gly590Val
CA346365375
NM_001382394.1:c.1769G>T