Canonical Allele Identifier: PA2828894979
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Asn1011Ser
CA136129
NM_001382395.1:c.3032A>G