Canonical Allele Identifier: PA2828893132
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 981557
ClinVar RCV Id: RCV001261070

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Asp196Gly
CA346373149
NM_001382394.1:c.587A>G