Canonical Allele Identifier: PA105048
Gene: SOS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 45361
ClinVar RCV Id: RCV000038549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005624.2:p.Pro112Arg
CA261741
NM_005633.4:c.335C>G