Canonical Allele Identifier: PA2828894555
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 981565
ClinVar RCV Id: RCV001261081

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Met468Thr
CA346366251
NM_001382395.1:c.1403T>C