Canonical Allele Identifier: PA645387020
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 376857
ClinVar RCV Id: RCV000429991 RCV000607638 RCV000652817 RCV003168619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.Thr1079Ala
CA7176854
NM_006939.4:c.3235A>G