Canonical Allele Identifier: PA2828893368
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2085827
ClinVar RCV Id: RCV002996470

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Asp458Gly
CA346366272
NM_001382394.1:c.1373A>G