Canonical Allele Identifier: PA105086
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 12869
ClinVar RCV Id: RCV000013729 RCV000038570 RCV000149833 RCV000213007 RCV000515403 RCV003450637
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Thr266Lys
CA256578
NM_005633.4:c.797C>A