Canonical Allele Identifier: PA2825301587
Gene: RSPH4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1362434
ClinVar RCV Id: RCV001932285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001010892.1:p.Arg336Cys
CA3970881
NM_001010892.3:c.1006C>T