Canonical Allele Identifier: PA2830069915
Gene: RSPH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1009986
ClinVar RCV Id: RCV001307552
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114130.4:p.Ala350delinsGlyPro
CA1676373905
NM_031924.8:c.1048_1049insGTC