Canonical Allele Identifier: PA658664929
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 475749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.Arg986Lys
CA7176917
NM_006939.4:c.2957G>A