Canonical Allele Identifier: PA2828893423
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 636446
ClinVar RCV Id: RCV000788277

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Asp513Val
CA346365892
NM_001382394.1:c.1538A>T