Canonical Allele Identifier: PA2828894574
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 180720
ClinVar RCV Id: RCV000157696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Ser484Arg
CA235358
NM_001382395.1:c.1452C>A
CA346366143
NM_001382395.1:c.1452C>G
CA346366149
NM_001382395.1:c.1450A>C