Canonical Allele Identifier: PA2828894362
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 496312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Ile252Thr
CA1624725
NM_001382395.1:c.755T>C