Canonical Allele Identifier: PA2828893176
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40660

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Val243Ala
CA136183
NM_001382394.1:c.728T>C