Canonical Allele Identifier: PA2828894490
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2813717
ClinVar RCV Id: RCV003655698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Glu402Asp
CA346366711
NM_001382395.1:c.1206A>T
CA346366712
NM_001382395.1:c.1206A>C