Canonical Allele Identifier: PA136157
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 45369
ClinVar RCV Id: RCV000038557 RCV003654186
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Gly1245Val
CA136155
NM_005633.4:c.3734G>T