Canonical Allele Identifier: PA2828893822
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 280646

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Met1043Val
CA10602858
NM_001382394.1:c.3127A>G