Canonical Allele Identifier: PA2828894017
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 45369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Gly1238Val
CA136155
NM_001382394.1:c.3713G>T