Canonical Allele Identifier: PA2828894613
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 860321
ClinVar RCV Id: RCV001066604

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Ser523Asn
CA346365871
NM_001382395.1:c.1568G>A