Canonical Allele Identifier: PA916003712
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 636446
ClinVar RCV Id: RCV000788277

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Asp520Val
CA346365892
NM_005633.4:c.1559A>T