Canonical Allele Identifier: PA2826724660
Gene: RSPH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 408126
ClinVar RCV Id: RCV000469271 RCV001333455 RCV002526411
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273435.1:p.Arg265Gly
CA10043694
NM_001286506.2:c.793A>G