Canonical Allele Identifier: PA2828893418
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2811691
ClinVar RCV Id: RCV003655688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Phe507Leu
CA1624587
NM_001382394.1:c.1519T>C
CA346365932
NM_001382394.1:c.1521T>G
CA346365933
NM_001382394.1:c.1521T>A