Canonical Allele Identifier: PA2828894634
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40678
ClinVar Variation Id: 40679

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Ser548Arg
CA234977
NM_001382395.1:c.1642A>C
CA297272
NM_001382395.1:c.1644T>A
CA346365700
NM_001382395.1:c.1644T>G