Canonical Allele Identifier: PA136192
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 45381
ClinVar RCV Id: RCV000038577 RCV000349172 RCV000394772 RCV001366413 RCV001567493 RCV002371837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Arg310His
CA136190
NM_005633.4:c.929G>A