Canonical Allele Identifier: PA2828893206
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Met262Thr
CA235344
NM_001382394.1:c.785T>C