Canonical Allele Identifier: PA1139704416
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 992452
ClinVar RCV Id: RCV001280902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Asn536Ser
CA346365782
NM_005633.4:c.1607A>G