Canonical Allele Identifier: PA658659159
Gene: SOS1 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Leu670Phe
CA1624490
NM_005633.4:c.2010G>C
CA346364870
NM_005633.4:c.2010G>T