Canonical Allele Identifier: PA2828893390
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721710
ClinVar RCV Id: RCV002294961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Asn478Lys
CA346366136
NM_001382394.1:c.1434T>G
CA346366137
NM_001382394.1:c.1434T>A