Canonical Allele Identifier: PA2828894693
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1695867
ClinVar RCV Id: RCV002265502 RCV002488661 RCV003096001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Glu590Asp
CA346365422
NM_001382395.1:c.1770G>C
CA346365423
NM_001382395.1:c.1770G>T