Canonical Allele Identifier: PA645396039
Gene: RSPH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 241790

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_543136.1:p.Ala244Thr
CA10043759
NM_080860.4:c.730G>A