Canonical Allele Identifier: PA645408049
Gene: RSPH4A HGNC NCBI

Linked Data

ClinVar Variation Id: 355125
ClinVar RCV Id: RCV000381582 RCV000593752 RCV002058555 RCV003972491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001010892.1:p.Glu701Gln
CA3971115
NM_001010892.3:c.2101G>C