Canonical Allele Identifier: PA2828894002
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 179112

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Pro1229Thr
CA183755
NM_001382394.1:c.3685C>A