Canonical Allele Identifier: PA1139704497
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 944819
ClinVar RCV Id: RCV001215308

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Ile610Val
CA1624545
NM_005633.4:c.1828A>G