Canonical Allele Identifier: PA2828894796
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Gly719Ala
CA297202
NM_001382395.1:c.2156G>C