Canonical Allele Identifier: PA2828893385
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40675
ClinVar RCV Id: RCV000612204

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Pro471Leu
CA346366180
NM_001382394.1:c.1412C>T