Canonical Allele Identifier: PA2828893439
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 992452
ClinVar RCV Id: RCV001280902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Asn529Ser
CA346365782
NM_001382394.1:c.1586A>G