Canonical Allele Identifier: PA915986517
Gene: RSPH4A HGNC NCBI

Linked Data

ClinVar Variation Id: 355121
ClinVar RCV Id: RCV000399601 RCV001095040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155136.1:p.Phe505Ser
CA3970965
NM_001161664.2:c.1514T>C