Canonical Allele Identifier: PA2828893429
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 860321
ClinVar RCV Id: RCV001066604

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Ser516Asn
CA346365871
NM_001382394.1:c.1547G>A