Canonical Allele Identifier: PA2826179209
Gene: RSPH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1444848
ClinVar RCV Id: RCV001982625 RCV002484741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180270.1:p.Ala94Val
CA3828268
NM_001193341.2:c.281C>T