Canonical Allele Identifier: PA2741934056
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2887770
ClinVar RCV Id: RCV003756209
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.Pro303Ser
CA389647034
NM_006939.4:c.907C>T