Canonical Allele Identifier: PA2828893526
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40688
ClinVar RCV Id: RCV000654972

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Met610Thr
CA1624541
NM_001382394.1:c.1829T>C