Canonical Allele Identifier: PA2828894711
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40688
ClinVar RCV Id: RCV000654972

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Met617Thr
CA1624541
NM_001382395.1:c.1850T>C