Canonical Allele Identifier: PA2828894614
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3016320
ClinVar RCV Id: RCV003876471

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369324.1:p.Ser523Arg
CA1624580
NM_001382395.1:c.1569T>G
CA346365869
NM_001382395.1:c.1569T>A
CA346365875
NM_001382395.1:c.1567A>C