Canonical Allele Identifier: PA177734
Gene: RSPH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 165063
ClinVar RCV Id: RCV000151749 RCV000464108 RCV001165017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689945.2:p.Val141Met
CA177733
NM_152732.5:c.421G>A