Canonical Allele Identifier: PA105097
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 181553

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Thr549Lys
CA297273
NM_005633.4:c.1646C>A