Canonical Allele Identifier: PA2830069855
Gene: RSPH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 475820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114130.4:p.Arg256Gln
CA4075820
NM_031924.8:c.767G>A