Canonical Allele Identifier: PA185041
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 179739
ClinVar RCV Id: RCV000156537 RCV000414349 RCV000770761 RCV000793245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Phe623Val
CA185039
NM_005633.4:c.1867T>G