Canonical Allele Identifier: PA183757
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 179112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Pro1236Thr
CA183755
NM_005633.4:c.3706C>A