Canonical Allele Identifier: PA136185
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Val250Ala
CA136183
NM_005633.4:c.749T>C