Canonical Allele Identifier: PA351652
Gene: SPRY2 HGNC NCBI

Linked Data

ClinVar Variation Id: 222032
ClinVar RCV Id: RCV000207508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005833.1:p.Arg119Trp
CA351651
NM_005842.4:c.355C>T