Canonical Allele Identifier: PA136145
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40733
ClinVar RCV Id: RCV000159143 RCV000459983 RCV000788015 RCV001269262 RCV002453289 RCV003974867
ClinVar Variation Id: 45365
ClinVar RCV Id: RCV000038553 RCV002272040 RCV003539774
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Asp1200Glu
CA136143
NM_005633.4:c.3600C>A
CA297240
NM_005633.4:c.3600C>G