Canonical Allele Identifier: PA2828894610
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 636446
ClinVar RCV Id: RCV000788277

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Asp520Val
CA346365892
NM_001382395.1:c.1559A>T