Canonical Allele Identifier: PA183767
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 179117
ClinVar RCV Id: RCV000155902 RCV000284494 RCV000376698 RCV000586070 RCV000654926 RCV000764405 RCV003448272 RCV003298167
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Val574Ile
CA183765
NM_005633.4:c.1720G>A