Canonical Allele Identifier: PA2826179275
Gene: RSPH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 357020
ClinVar RCV Id: RCV000265038 RCV001095134
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180270.1:p.Leu291Phe
CA3828430
NM_001193341.2:c.871C>T