Canonical Allele Identifier: PA2573304618
Gene: RSPH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1477175
ClinVar RCV Id: RCV001971461
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689945.2:p.Glu110Lys
CA3828277
NM_152732.5:c.328G>A