Canonical Allele Identifier: PA2826179218
Gene: RSPH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1477175
ClinVar RCV Id: RCV001971461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180270.1:p.Glu110Lys
CA3828277
NM_001193341.2:c.328G>A