Canonical Allele Identifier: PA645407971
Gene: RSPH4A HGNC NCBI

Linked Data

ClinVar Variation Id: 355124
ClinVar RCV Id: RCV000271851 RCV000598056 RCV001095101 RCV003932466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001010892.1:p.Pro664Ser
CA3971101
NM_001010892.3:c.1990C>T