Canonical Allele Identifier: PA2828894684
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2111180
ClinVar RCV Id: RCV003045872

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Glu583Val
CA346365473
NM_001382395.1:c.1748A>T