Canonical Allele Identifier: PA2580526335
Gene: RSPH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1732688
ClinVar RCV Id: RCV002339775
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689945.2:p.Val119Met
CA3828280
NM_152732.5:c.355G>A