Canonical Allele Identifier: PA2828894238
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 45361
ClinVar RCV Id: RCV000038549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Pro112Arg
CA261741
NM_001382395.1:c.335C>G