Canonical Allele Identifier: PA2580167987
Gene: RSPH4A HGNC NCBI

Linked Data

ClinVar Variation Id: 1715473
ClinVar RCV Id: RCV002301259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155136.1:p.Tyr321Asn
CA365403078
NM_001161664.2:c.961T>A