Canonical Allele Identifier: PA658818584
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 506639
ClinVar RCV Id: RCV000610376 RCV000792762 RCV002431764
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.Asn867Ser
CA7177004
NM_006939.4:c.2600A>G