Canonical Allele Identifier: PA177731
Gene: RSPH4A HGNC NCBI

Linked Data

ClinVar Variation Id: 165062
ClinVar RCV Id: RCV000151748 RCV000311643 RCV001095099 RCV001706006
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001010892.1:p.Asn627His
CA177730
NM_001010892.3:c.1879A>C