Canonical Allele Identifier: PA2580474624
Gene: RSPH6A HGNC NCBI

Linked Data

ClinVar Variation Id: 2305325
ClinVar RCV Id: RCV004151141

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110412.1:p.Glu510Val
CA406404822
NM_030785.4:c.1529A>T