Canonical Allele Identifier: PA2573304616
Gene: RSPH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1444848
ClinVar RCV Id: RCV001982625 RCV002484741
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689945.2:p.Ala94Val
CA3828268
NM_152732.5:c.281C>T