Canonical Allele Identifier: PA2828893203
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 12870

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Met262Arg
CA235346
NM_001382394.1:c.785T>G