Canonical Allele Identifier: PA2499275398
Gene: SOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1005668
ClinVar RCV Id: RCV001302584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008870.2:p.Arg153Gln
CA7177522
NM_006939.4:c.458G>A