Canonical Allele Identifier: PA2828893601
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40697

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Ala701Thr
CA136094
NM_001382394.1:c.2101G>A