Canonical Allele Identifier: PA2828894568
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2097848
ClinVar RCV Id: RCV003006465

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Pro478Ser
CA346366183
NM_001382395.1:c.1432C>T