Canonical Allele Identifier: PA105028
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 636262
ClinVar RCV Id: RCV000788001 RCV000856753 RCV001196815 RCV003313978 RCV003166075
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Phe623Ile
CA346365197
NM_005633.4:c.1867T>A