Canonical Allele Identifier: PA2828894361
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Val250Ala
CA136183
NM_001382395.1:c.749T>C