Canonical Allele Identifier: PA2826179206
Gene: RSPH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1408243
ClinVar RCV Id: RCV001909455
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180270.1:p.Glu91Gln
CA364288468
NM_001193341.2:c.271G>C