Canonical Allele Identifier: PA915986453
Gene: RSPH4A HGNC NCBI

Linked Data

ClinVar Variation Id: 178799
ClinVar RCV Id: RCV000155567 RCV000293332 RCV001095097 RCV001706054
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155136.1:p.Thr149Ser
CA183058
NM_001161664.2:c.446C>G
CA365393349
NM_001161664.2:c.445A>T