Canonical Allele Identifier: PA2828894172
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Thr37Ala
CA136074
NM_001382395.1:c.109A>G