Canonical Allele Identifier: PA2828893391
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 632997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Asn478Ser
CA45674752
NM_001382394.1:c.1433A>G