Canonical Allele Identifier: PA2741924639
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2811691
ClinVar RCV Id: RCV003655688

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Phe514Leu
CA1624587
NM_005633.4:c.1540T>C
CA346365932
NM_005633.4:c.1542T>G
CA346365933
NM_005633.4:c.1542T>A