Canonical Allele Identifier: PA2828893533
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 179739

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Phe616Val
CA185039
NM_001382394.1:c.1846T>G