Canonical Allele Identifier: PA181529
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40640
ClinVar RCV Id: RCV000154848 RCV000521504 RCV001711220 RCV002381283 RCV002482943 RCV003934876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Pro25Ser
CA181527
NM_005633.4:c.73C>T