Canonical Allele Identifier: PA2828893386
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2097848
ClinVar RCV Id: RCV003006465

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369323.1:p.Pro471Ser
CA346366183
NM_001382394.1:c.1411C>T