Canonical Allele Identifier: PA2826179238
Gene: RSPH9 HGNC NCBI

Linked Data

ClinVar Variation Id: 357018
ClinVar RCV Id: RCV000360854 RCV001095288 RCV003932472
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180270.1:p.Arg156Gln
CA3828314
NM_001193341.2:c.467G>A