Canonical Allele Identifier: PA645386987
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 209091
ClinVar RCV Id: RCV000191030 RCV000224178 RCV000845122 RCV003454490
ClinVar Variation Id: 684625
ClinVar RCV Id: RCV000845123 RCV003223414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.Thr376Ser
CA358853
NM_006939.4:c.1127C>G
CA16021005
NM_006939.4:c.1126A>T