Canonical Allele Identifier: PA136122
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 45357
ClinVar RCV Id: RCV000038541 RCV000654932 RCV000586941 RCV001143052 RCV001138300 RCV002433506
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Arg989Lys
CA136120
NM_005633.4:c.2966G>A