Canonical Allele Identifier: PA2828893497
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1365663

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Pro573Arg
CA346365493
NM_001382394.1:c.1718C>G