Canonical Allele Identifier: PA104816
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Arg552Met
CA16616762
NM_005633.4:c.1655G>T