Canonical Allele Identifier: PA2828893389
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 180720
ClinVar RCV Id: RCV000157696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Ser477Arg
CA235358
NM_001382394.1:c.1431C>A
CA346366143
NM_001382394.1:c.1431C>G
CA346366149
NM_001382394.1:c.1429A>C