Canonical Allele Identifier: PA1139703997
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 981563
ClinVar RCV Id: RCV001261078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Leu417Pro
CA346366603
NM_005633.4:c.1250T>C