Canonical Allele Identifier: PA2828893026
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Phe71Cys
CA297244
NM_001382394.1:c.212T>G