Canonical Allele Identifier: PA645387321
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 372656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Arg552Trp
CA16042455
NM_005633.4:c.1654A>T