Canonical Allele Identifier: PA658818554
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 542398
ClinVar RCV Id: RCV000652814 RCV001175494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.Ala208Ser
CA7177485
NM_006939.4:c.622G>T