Allele Registry

Canonical Allele Identifier: PA645386987

Gene: SOS2 HGNC NCBI

ClinVar RCV:

RCV000191030

RCV000224178

RCV000845122

RCV000845123

RCV003223414

RCV003454490

ClinVar Variation:

209091

684625

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