Canonical Allele Identifier: PA2580337562
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2202335
ClinVar RCV Id: RCV002647939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.Pro1083Ser
CA389640556
NM_006939.4:c.3247C>T