Canonical Allele Identifier: PA2826724631
Gene: RSPH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 241790

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273435.1:p.Ala206Thr
CA10043759
NM_001286506.2:c.616G>A