Canonical Allele Identifier: PA2828893338
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Glu426Lys
CA235348
NM_001382394.1:c.1276G>A