Canonical Allele Identifier: PA2828894688
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 449125
ClinVar RCV Id: RCV000520823

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Ile587Thr
CA346365446
NM_001382395.1:c.1760T>C