Canonical Allele Identifier: PA136076
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40641
ClinVar RCV Id: RCV000038509 RCV000159147 RCV001143269 RCV001143267 RCV001703446 RCV001813278 RCV002453283 RCV003904889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Thr37Ala
CA136074
NM_005633.4:c.109A>G