Canonical Allele Identifier: PA2828894575
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721710
ClinVar RCV Id: RCV002294961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Asn485Lys
CA346366136
NM_001382395.1:c.1455T>G
CA346366137
NM_001382395.1:c.1455T>A