Canonical Allele Identifier: PA261745
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 45373

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Val171Ala
CA261743
NM_005633.4:c.512T>C