Canonical Allele Identifier: PA2828893500
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2111180
ClinVar RCV Id: RCV003045872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Glu576Val
CA346365473
NM_001382394.1:c.1727A>T